Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran (Q27317126)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26445815%20AND%20SRC:MED&resulttype=core&format=json

26 February 2020

title

Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran (English)

1 reference

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26 February 2020

1 reference

1 reference

28

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26 February 2020

Hasan Otukesh

18

1 reference

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26 February 2020

Ahmad Daneshi

23

1 reference

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26 February 2020

Mohammad Farhadi

24

1 reference

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26 February 2020

Kimia Kahrizi

25

1 reference

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26 February 2020

Richard J Smith

26

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26 February 2020

author name string

Christina M Sloan-Heggen

1

1 reference

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26 February 2020

Mojgan Babanejad

2

1 reference

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26 February 2020

Maryam Beheshtian

3

1 reference

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26 February 2020

Allen C Simpson

4

1 reference

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26 February 2020

Kevin T Booth

5

1 reference

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26 February 2020

Fariba Ardalani

6

1 reference

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26 February 2020

Kathy L Frees

7

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26 February 2020

Marzieh Mohseni

8

1 reference

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26 February 2020

Reza Mozafari

9

1 reference

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26 February 2020

Zohreh Mehrjoo

10

1 reference

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26 February 2020

Leila Jamali

11

1 reference

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26 February 2020

Saeideh Vaziri

12

1 reference

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26 February 2020

Tara Akhtarkhavari

13

1 reference

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26 February 2020

Niloofar Bazazzadegan

14

1 reference

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26 February 2020

Nooshin Nikzat

15

1 reference

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26 February 2020

Sanaz Arzhangi

16

1 reference

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26 February 2020

Farahnaz Sabbagh

17

1 reference

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26 February 2020

Seyed Morteza Seifati

19

1 reference

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26 February 2020

Hossein Khodaei

20

1 reference

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26 February 2020

Maryam Taghdiri

21

1 reference

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26 February 2020

Nicole C Meyer

22

1 reference

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26 February 2020

Hela Azaiez

27

1 reference

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26 February 2020

language of work or name

English

0 references

publication date

7 October 2015

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26445815%20AND%20SRC:MED&resulttype=core&format=json

Journal of Medical Genetics

26 February 2020

published in

1 reference

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26 February 2020

volume

52

1 reference

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26 February 2020

issue

12

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26 February 2020

page(s)

823-829

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PDZD7 and hearing loss: More than just a modifier

26 February 2020

cites work

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Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans

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Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus

21 March 2017

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Genetic analysis through OtoSeq of Pakistani families segregating prelingual hearing loss

28 September 2017

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Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in Middle Eastern families

28 September 2017

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Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations

28 September 2017

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28 September 2017

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Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families

28 September 2017

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28 September 2017

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Molecular analysis of SLC26A4 gene in patients with nonsyndromic hearing loss and EVA: identification of two novel mutations in Brazilian patients

21 January 2018

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Analysis of the thyroid phenotype in 42 patients with Pendred syndrome and nonsyndromic enlargement of the vestibular aqueduct.

21 January 2018

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Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment

21 January 2018

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GJB2 mutations: passage through Iran

21 January 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/26445815

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26445815

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMEDGENET-2015-103389

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26445815%20AND%20SRC:MED&resulttype=core&format=json

26 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26445815%20AND%20SRC:MED&resulttype=core&format=json

26 February 2020

1 reference