Novel compound heterozygous mutations in the PARK2 gene identified in a Chinese pedigree with early‐onset Parkinson's disease

OBJECTS: To capture point mutations and short insertions/deletions in 49 previously reported genes associated with Parkinson's disease (PD) in a Chinese pedigree with early‐onset Parkinson's disease (EOPD)‐affected individuals. METHODS: Clinical examinations and genomic analysis were perfo...

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Detalles Bibliográficos
Autores principales: Shi, Yingying, Kawakami, Hideshi, Zang, Weizhou, Li, Gang, Zhang, Jiewen, Xu, Changshui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5853629/
https://www.ncbi.nlm.nih.gov/pubmed/29568695
http://dx.doi.org/10.1002/brb3.901

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5853629/
https://www.ncbi.nlm.nih.gov/pubmed/29568695
http://dx.doi.org/10.1002/brb3.901

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