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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Detalles Bibliográficos
Autores principales: Huang, Ting, Gao, Chen‐Yu, Wu, Liang, Gong, Peng‐Yu, Wang, Ji‐Zheng, Tian, You‐Yong, Zhang, Ying‐Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6749482/
https://www.ncbi.nlm.nih.gov/pubmed/31386307
http://dx.doi.org/10.1002/brb3.1372

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6749482/
https://www.ncbi.nlm.nih.gov/pubmed/31386307
http://dx.doi.org/10.1002/brb3.1372

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