Novel A18T and pA29S substitutions in α-synuclein may be associated with sporadic Parkinson's disease

OBJECTIVE: Mutations in the α-synuclein-encoding gene SNCA are considered as a rare cause of Parkinson's disease (PD). Our objective was to examine the frequency of the SNCA point mutations among PD patients of Polish origin. METHODS: Detection of the known SNCA point mutations A30P (c.88G>C...

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Detalhes bibliográficos
Principais autores: Hoffman-Zacharska, Dorota, Koziorowski, Dariusz, Ross, Owen A., Milewski, Micha 1, Poznanski, Jaros 1 aw, Jurek, Marta, Wszolek, Zbigniew K., Soto-Ortolaza, Alexandra, awek, Jaros 1 aw S 1, Janik, Piotr, Jamrozik, Zygmunt, Potulska-Chromik, Anna, Jasinska-Myga, Barbara, Opala, Grzegorz, Krygowska-Wajs, Anna, Czyzewski, Krzysztof, Dickson, Dennis W., Bal, Jerzy, Friedman, Andrzej
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4055791/
https://ncbi.nlm.nih.gov/pubmed/23916651
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.parkreldis.2013.07.011
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