Quelle information à donner aux patients atteints de SLA porteurs de la mutation c9orf72 ?
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference12 articles.
1. Mutation in c9orf72 changes the boundaries of ALS and FTD;Andersen;Lancet Neurol,2012
2. Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a c9orf72 repeat expansion: a population-based cohort study;Byrne;Lancet Neurol,2012
3. Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of c9orf72;Chio;Brain,2012
4. Expanded GGGGCC hexanucleotide repeat in noncoding region of c9orf72 causes chromosome 9p-linked FTD and ALS;Dejesus-Hernandez;Neuron,2011
5. Familial fronto-temporal dementia and amyotrophic lateral sclerosis associated with the c9orf72 hexanucleotide repeat;Hodges;Brain,2012
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