Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis

Published:2013-09 Issue:9 Volume:34 Page:2234.e13-2234.e19
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Harms Matthew B.,Cady Janet,Zaidman Craig,Cooper Paul,Bali Taha,Allred Peggy,Cruchaga Carlos,Baughn Michael,Libby Ryan T.,Pestronk Alan,Goate Alison,Ravits John,Baloh Robert H.

Funder

National Institutes of Health (NIH)

National Center for Research Resources (NCRR)

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Clinical Neurology,Ageing,General Neuroscience

Reference35 articles.

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4. Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72;Chiò;Brain,2012

5. Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72;Cooper-Knock;Brain,2012

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