Lack of unique neuropathology in amyotrophic lateral sclerosis associated with p.K54E angiogenin (ANG) mutation

AIMS: Five to 10% of cases of amyotrophic lateral sclerosis are familial, with the most common genetic causes being mutations in the C9ORF72, SOD1, TARDBP and FUS genes. Mutations in the angiogenin gene, ANG, have been identified in both familial and sporadic patients in several populations within E...

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Detalhes bibliográficos
Main Authors: Kirby, J, Highley, J R, Cox, L, Goodall, E F, Hewitt, C, Hartley, J A, Hollinger, H C, Fox, M, Ince, P G, McDermott, C J, Shaw, P J
Formato: Artigo
Idioma:Inglês
Publicado em: Blackwell Publishing Ltd 2013
Assuntos:
Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3770927/
https://ncbi.nlm.nih.gov/pubmed/23228179
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/nan.12007
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