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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770927/
https://www.ncbi.nlm.nih.gov/pubmed/23228179
http://dx.doi.org/10.1111/nan.12007

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770927/
https://www.ncbi.nlm.nih.gov/pubmed/23228179
http://dx.doi.org/10.1111/nan.12007

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