Whole exome analysis identifies frequent CNGA1 mutations in Japanese population with autosomal recessive retinitis pigmentosa (Q34277608)

1 August 2017

Whole exome analysis identifies frequent CNGA1 mutations in Japanese population with autosomal recessive retinitis pigmentosa (English)

1 reference

1 August 2017

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25268133%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

Yoshinori Tsurusaki

13

1 reference

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4 June 2020

5

Kazuho Ikeo

1 reference

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4 June 2020

author name string

Masakazu Akahori

2

1 reference

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4 June 2020

Yuri Sergeev

3

1 reference

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4 June 2020

Kazutoshi Yoshitake

4

1 reference

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4 June 2020

Masaaki Furuno

6

1 reference

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4 June 2020

Takaaki Hayashi

7

1 reference

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4 June 2020

Mineo Kondo

8

1 reference

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4 June 2020

Shinji Ueno

9

1 reference

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4 June 2020

Kazushige Tsunoda

10

1 reference

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4 June 2020

Kei Shinoda

11

1 reference

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4 June 2020

Kazuki Kuniyoshi

12

1 reference

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4 June 2020

Naomichi Matsumoto

14

1 reference

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4 June 2020

Hiroshi Tsuneoka

15

1 reference

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4 June 2020

Takeshi Iwata

16

1 reference

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4 June 2020

language of work or name

English

0 references

publication date

30 September 2014

1 reference

1 August 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25268133%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

volume

9

1 reference

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4 June 2020

page(s)

e108721

1 reference

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4 June 2020

issue

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25268133%20AND%20SRC:MED&resulttype=core&format=json

Creative Commons Attribution 4.0 International

4 June 2020

copyright license

start time

30 September 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Whole-exome sequencing identifies a novel ALMS1 mutation (p.Q2051X) in two Japanese brothers with Alström syndrome

1 reference

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Two novel mutations in the EYS gene are possible major causes of autosomal recessive retinitis pigmentosa in the Japanese population

6 July 2018

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High prevalence of mutations in the EYS gene in Japanese patients with autosomal recessive retinitis pigmentosa

6 July 2018

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Mutation screening of multiple genes in Spanish patients with autosomal recessive retinitis pigmentosa by targeted resequencing

6 July 2018

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Mutations in C2ORF71 cause autosomal-recessive retinitis pigmentosa

6 July 2018

1 reference

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EYS is a major gene for rod-cone dystrophies in France.

6 July 2018

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Identification of novel mutations in the ortholog of Drosophila eyes shut gene (EYS) causing autosomal recessive retinitis pigmentosa.

6 July 2018

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Fast and accurate short read alignment with Burrows-Wheeler transform

6 July 2018

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Next-generation DNA sequencing techniques

6 July 2018

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Identification of a 2 Mb human ortholog of Drosophila eyes shut/spacemaker that is mutated in patients with retinitis pigmentosa

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182560

Next-generation DNA sequencing

6 July 2018

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EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa

6 July 2018

1 reference

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Next-generation DNA sequencing methods

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The impact of next-generation sequencing technology on genetics

6 July 2018

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6 July 2018

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Autosomal recessive retinitis pigmentosa in a Pakistani family mapped to CNGA1 with identification of a novel mutation

6 July 2018

1 reference

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Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone-rod dystrophy and retinitis pigmentosa

6 July 2018

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Novel homozygous mutation in the alpha subunit of the rod cGMP gated channel (CNGA1) in two Spanish sibs affected with autosomal recessive retinitis pigmentosa

6 July 2018

1 reference

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Missense mutation in the USH2A gene: association with recessive retinitis pigmentosa without hearing loss

6 July 2018

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Retinitis pigmentosa and progressive sensorineural hearing loss caused by a C12258A mutation in the mitochondrial MTTS2 gene

6 July 2018

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Recessive mutations in the gene encoding the tubby-like protein TULP1 in patients with retinitis pigmentosa

6 July 2018

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6 July 2018

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Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci

6 July 2018

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A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese

6 July 2018

1 reference

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Mutations in the gene encoding the alpha subunit of the rod cGMP-gated channel in autosomal recessive retinitis pigmentosa

6 July 2018

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Point mutations of rhodopsin gene found in Japanese families with autosomal dominant retinitis pigmentosa (ADRP)

6 July 2018

1 reference

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Novel null mutations in the EYS gene are a frequent cause of autosomal recessive retinitis pigmentosa in the Israeli population

6 July 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0108721

Identifying pathogenic genetic background of simplex or multiplex retinitis pigmentosa patients: a large scale mutation screening study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0108721

Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0108721

Targeted sequencing of 179 genes associated with hereditary retinal dystrophies and 10 candidate genes identifies novel and known mutations in patients with various retinal diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0108721

Arrestin gene mutations in autosomal recessive retinitis pigmentosa

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182560

Autosomal dominant retinitis pigmentosa. A mutation in codon 181 (Glu-->Lys) of the rhodopsin gene in a Japanese family

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25268133

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Missense mutation of rhodopsin gene codon 15 found in Japanese autosomal dominant retinitis pigmentosa

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25268133

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0108721

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25268133%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25268133%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25268133%20AND%20SRC:MED&resulttype=core&format=json