UBQLN2 mutations are rare in French and French–Canadian amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

UBQLN2 mutations are rare in French and French–Canadian amyotrophic lateral sclerosis

Published:2012-09 Issue:9 Volume:33 Page:2230.e1-2230.e5
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Daoud Hussein,Suhail Hamid,Szuto Anna,Camu William,Salachas Francois,Meininger Vincent,Bouchard Jean-Pierre,Dupré Nicolas,Dion Patrick A.,Rouleau Guy A.

Publisher

Elsevier BV

Subject

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

Reference12 articles.

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2. Motor neuron disease: A role for ubiquilin 2 mutations in neurodegeneration;Daoud;Nature reviews Neurology,2011

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

4. Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia;Deng;Nature,2011

5. 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

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