(Q36508172)

14 August 2017

C9ORF72 expansion is not a significant cause of sporadic spinocerebellar ataxia (English)

1 reference

14 August 2017

5

Daniel H Geschwind

1 reference

14 August 2017

Brent L Fogel

1

1 reference

14 August 2017

Mochtar Pribadi

2

1 reference

14 August 2017

Sarah Pi

3

1 reference

14 August 2017

Susan L Perlman

4

1 reference

14 August 2017

Giovanni Coppola

6

1 reference

14 August 2017

language of work or name

English

0 references

publication date

18 October 2012

1 reference

14 August 2017

1 reference

14 August 2017

27

1 reference

14 August 2017

14

1 reference

14 August 2017

1832-1833

1 reference

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3536912

Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3536912

Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3536912

The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3536912

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3536912

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3536912

Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3536912

21 September 2018

Identifiers

DOI

10.1002/MDS.25245

1 reference

14 August 2017

1 reference

14 August 2017

PubMed publication ID

23080112

1 reference