Han Chinese family with early‐onset Parkinson's disease carries novel compound heterozygous mutations in the PARK2 gene

PURPOSE: To identify deletions, duplications, and point mutations in 55 previously reported genes associated with Parkinson's disease (PD) and certain genes associated with tremor, spinocerebellar ataxia, and dystonia in a Han Chinese pedigree with early‐onset Parkinson's disease (EOPD). P...

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Detalhes bibliográficos
Publicado no:Brain Behav
Main Authors: Huang, Ting, Gao, Chen‐Yu, Wu, Liang, Gong, Peng‐Yu, Wang, Ji‐Zheng, Tian, You‐Yong, Zhang, Ying‐Dong
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2019
Assuntos:
Original Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6749482/
https://ncbi.nlm.nih.gov/pubmed/31386307
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/brb3.1372
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