FUS mutations in sporadic amyotrophic lateral sclerosis (Q33937517)

30 July 2017

FUS mutations in sporadic amyotrophic lateral sclerosis (English)

1 reference

amyotrophic lateral sclerosis

30 July 2017

0 references

6

Allissa Dillman

0 references

Rossella Spataro

Rossella Spataro

13

0 references

Jessica Mandrioli

Jessica Mandrioli

19

0 references

Stefania Battistini

Stefania Battistini

9

0 references

Claudia Caponnetto

Claudia Caponnetto

11

0 references

Andrea Calvo

Andrea Calvo

8

0 references

Mario Sabatelli

Mario Sabatelli

17

0 references

Gianluigi Mancardi

Giovanni Luigi Mancardi

12

0 references

Mark R Cookson

7

Mark Cookson

1 reference

30 July 2017

25

Gabriele Mora

1 reference

30 July 2017

27

Adriano Chiò

1 reference

30 July 2017

26

Gabriella Restagno

1 reference

30 July 2017

Maria Rosaria Monsurrò

14

Maria Rosaria Monsurro

1 reference

30 July 2017

28

Bryan J Traynor

1 reference

30 July 2017

15

Gioacchino Tedeschi

1 reference

30 July 2017

20

Patrizia Sola

1 reference

30 July 2017

Shiao-Lin Lai

1

1 reference

30 July 2017

Yevgeniya Abramzon

2

1 reference

30 July 2017

Jennifer C Schymick

3

1 reference

30 July 2017

Dietrich A Stephan

4

1 reference

30 July 2017

Travis Dunckley

5

1 reference

30 July 2017

Fabio Giannini

10

1 reference

30 July 2017

Kalliopi Marinou

16

1 reference

30 July 2017

Amelia Conte

18

1 reference

30 July 2017

Fabrizio Salvi

21

1 reference

30 July 2017

Ilaria Bartolomei

22

1 reference

30 July 2017

Federica Lombardo

23

1 reference

30 July 2017

ITALSGEN Consortium

24

1 reference

30 July 2017

6 February 2010

1 reference

30 July 2017

Neurobiology of Aging

1 reference

30 July 2017

32

1 reference

30 July 2017

3

1 reference

30 July 2017

550.e1-4

1 reference

Mutations in FUS cause FALS and SALS in French and French Canadian populations

30 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2891336

Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2891336

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2891336

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2891336

Genetics of familial amyotrophic lateral sclerosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2891336

Synonymous mutations in CFTR exon 12 affect splicing and are not neutral in evolution.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2891336

A human genome diversity cell line panel

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2891336

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2891336

Mutations affecting mRNA splicing are the most common molecular defects in patients with neurofibromatosis type 1.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2891336

El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis. Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases a

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2891336

A rare polymorphism in the low density lipoprotein (LDL) gene that affects mRNA splicing

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20138404

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Mutations of FUS gene in sporadic amyotrophic lateral sclerosis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20138404

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Prevalence of SOD1 mutations in the Italian ALS population

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20138404

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.NEUROBIOLAGING.2009.12.020

1 reference

30 July 2017

1 reference

30 July 2017

1 reference