Large C9orf72 Hexanucleotide Repeat Expansions Are Seen in Multiple Neurodegenerative Syndromes and Are More Frequent Than Expected in the UK Population-Reference-Cited by-同舟云学术

Large C9orf72 Hexanucleotide Repeat Expansions Are Seen in Multiple Neurodegenerative Syndromes and Are More Frequent Than Expected in the UK Population

Published:2013-03 Issue:3 Volume:92 Page:345-353
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Beck Jon,Poulter Mark,Hensman Davina,Rohrer Jonathan D.,Mahoney Colin J.,Adamson Gary,Campbell Tracy,Uphill James,Borg Aaron,Fratta Pietro,Orrell Richard W.,Malaspina Andrea,Rowe James,Brown Jeremy,Hodges John,Sidle Katie,Polke James M.,Houlden Henry,Schott Jonathan M.,Fox Nick C.,Rossor Martin N.,Tabrizi Sarah J.,Isaacs Adrian M.,Hardy John,Warren Jason D.,Collinge John,Mead Simon

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference25 articles.

1. A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD;Renton;Neuron,2011

2. Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS;DeJesus-Hernandez;Neuron,2011

3. A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: A gene identification study;Gijselinck;Lancet Neurol.,2012

4. Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: A cross-sectional study;Majounie;Lancet Neurol.,2012

5. The C9ORF72 expansion mutation has a single European founder that arose from a background haplotype associated with repeat instability;Smith;Dement. Geriatr. Cogn. Disord.,2012

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