(Q37265449)

19 August 2017

C9ORF72 transcription in a frontotemporal dementia case with two expanded alleles (English)

1 reference

19 August 2017

0 references

frontotemporal dementia

1 reference

Joanna J Bury

5

0 references

Natalie Connor-Robson

Natalie Connor-Robson

3

0 references

Johnathan Cooper-Knock

Johnathan Cooper-Knock

1

0 references

Janine Kirby

Janine Kirby

6

0 references

Pamela Shaw

Pamela J Shaw

9

0 references

author name string

Adrian Higginbottom

2

1 reference

19 August 2017

Nadhim Bayatti

4

1 reference

19 August 2017

Natalia Ninkina

7

1 reference

19 August 2017

Vladimir L Buchman

8

1 reference

19 August 2017

language of work or name

English

0 references

publication date

9 October 2013

1 reference

19 August 2017

1 reference

19 August 2017

81

1 reference

19 August 2017

19

1 reference

19 August 2017

1719-1721

1 reference

Hypermethylation of the CpG island near the G4C2 repeat in ALS with a C9orf72 expansion

19 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3812108

Simultaneous and independent detection of C9ORF72 alleles with low and high number of GGGGCC repeats using an optimised protocol of Southern blot hybridisation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3812108

Misregulated RNA processing in amyotrophic lateral sclerosis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3812108

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3812108

Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3812108

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3812108

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3812108

C9ORF72 hexanucleotide expansions of 20-22 repeats are associated with frontotemporal deterioration

6 September 2017

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24107864

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1212/01.WNL.0000435295.41974.2E

1 reference

19 August 2017

1 reference

19 August 2017

1 reference