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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Библиографические подробности
Опубликовано в: :Lancet Neurol
Главные авторы: 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
Формат: Artigo
Язык:Inglês
Опубликовано: 2013
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Article
Online-ссылка: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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