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PINK1 mutation heterozygosity and the risk of Parkinson's disease

BACKGROUND: Mutations in the PTEN‐induced kinase 1 (PINK1) gene have been identified in recessively inherited and sporadic early‐onset parkinsonism (EOP). METHODS: A total of 131 Norwegian patients diagnosed with Parkinson's disease were included. Of them, 89 participants had EOP (onset ⩽50 yea...

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Detalhes bibliográficos
Main Authors: Toft, M, Myhre, R, Pielsticker, L, White, L R, Aasly, J O, Farrer, M J
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2007
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2117782/
https://ncbi.nlm.nih.gov/pubmed/17172567
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.2006.097840
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