Screening for VPS35 mutations in Parkinson's disease

Recently 2 groups have independently identified a mutation in the gene ‘vacuolar protein sorting 35 homolog’ (VPS35 c.1858G>A; p.Asp620Asn) as a possible cause of autosomal dominant Parkinson's disease (PD). In order to assess the frequency of the reported mutation and to search for other po...

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Detalhes bibliográficos
Main Authors: Sheerin, Una-Marie, Charlesworth, Gavin, Bras, Jose, Guerreiro, Rita, Bhatia, Kailash, Foltynie, Thomas, Limousin, Patricia, Silveira-Moriyama, Laura, Lees, Andrew, Wood, Nicholas
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2012
Assuntos:
Genetic Reports Abstract
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3629567/
https://ncbi.nlm.nih.gov/pubmed/22154191
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neurobiolaging.2011.10.032
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