(Q34274164)

1 August 2017

A de novo missense mutation of the FUS gene in a "true" sporadic ALS case (English)

1 reference

amyotrophic lateral sclerosis

1 August 2017

1 reference

1

Adriano Chiò

1 reference

1 August 2017

3

Cristina Moglia

1 reference

1 August 2017

10

Gabriella Restagno

1 reference

1 August 2017

5

Maura Brunetti

1 reference

1 August 2017

9

Bryan J Traynor

1 reference

1 August 2017

Andrea Calvo

2

1 reference

1 August 2017

Irene Ossola

4

1 reference

1 August 2017

Luca Sbaiz

6

1 reference

1 August 2017

Shiao-lin Lai

7

1 reference

1 August 2017

Yevgeniya Abramzon

8

1 reference

1 August 2017

3 July 2010

1 reference

1 August 2017

Neurobiology of Aging

1 reference

1 August 2017

32

1 reference

1 August 2017

3

1 reference

1 August 2017

553.e23-6

1 reference

De novo truncating FUS gene mutation as a cause of sporadic amyotrophic lateral sclerosis

1 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2972379

FUS mutations in sporadic amyotrophic lateral sclerosis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2972379

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2972379

Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2972379

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2972379

Recent advances in the genetics of amyotrophic lateral sclerosis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2972379

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2972379

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2972379

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2972379

Estimate of the mutation rate per nucleotide in humans

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2972379

Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2972379

FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2972379

C-terminal FUS/TLS mutations in familial and sporadic ALS in Germany

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2972379

FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2972379

?True? sporadic ALS associated with a novel SOD-1 mutation

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2972379

Prevalence of SOD1 mutations in the Italian ALS population

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20598774

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/20598774

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.NEUROBIOLAGING.2010.05.016

1 reference

1 August 2017

1 reference

1 August 2017

1 reference