FXN GAA repeat expansions in amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

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FXN GAA repeat expansions in amyotrophic lateral sclerosis

Published:2014-08 Issue:8 Volume:21 Page:1319-1322
ISSN:0967-5868
Container-title:Journal of Clinical Neuroscience
language:en
Short-container-title:Journal of Clinical Neuroscience

Author:

Rizik Naji,Freischmidt Axel,Ludolph Albert C.,Weishaupt Jochen H.

Funder

German Federal Ministry of Education and Research

Charcot Foundation for ALS Research (ACL, JHW)

virtual Helmholtz Institute

Publisher

Elsevier BV

Subject

Physiology (medical),Clinical Neurology,Neurology,General Medicine,Surgery

Reference23 articles.

1. Frontotemporal dementia and motor neurone disease: overlapping clinic-pathological disorders;Lillo;J Clin Neurosci,2009

2. Clinical genetics of amyotrophic lateral sclerosis: what do we really know?;Andersen;Nat Rev Neurol,2011

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

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

5. Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS;Elden;Nature,2010

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