Controversies and priorities in amyotrophic lateral sclerosis

Two decades after the discovery that 20% of familial amyotrophic lateral sclerosis (ALS) cases were linked to mutations in the superoxide dismutase-1 (SOD1) gene, a substantial proportion of the remainder of cases of familial ALS have now been traced to an expansion of the intronic hexanucleotide re...

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Detalhes bibliográficos
Publicado no:Lancet Neurol
Main Authors: Turner, Martin R, Hardiman, Orla, Benatar, Michael, Brooks, Benjamin R, Chio, Adriano, de Carvalho, Mamede, Ince, Paul G, Lin, Cindy, Miller, Robert G, Mitsumoto, Hiroshi, Nicholson, Garth, Ravits, John, Shaw, Pamela J, Swash, Michael, Talbot, Kevin, Traynor, Bryan J, den Berg, Leonard H Van, Veldink, Jan H, Vucic, Steve, Kiernan, Matthew C
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4565161/
https://ncbi.nlm.nih.gov/pubmed/23415570
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/S1474-4422(13)70036-X
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