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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Lancet Neurol
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2013
Gaiak:
Article
Sarrera elektronikoa: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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