Genetic analysis of ATP13A2, PLA2G6 and FBXO7 in a cohort of Chinese patients with early-onset Parkinson’s disease

Several genes have already been certified as causative genes in patients with autosomal recessive early-onset Parkinson’s syndrome with pyramidal tract signs, including ATP13A2, PLA2G6 and FBXO7. Variants in these three genes may also play roles in early-onset Parkinson’s disease (EOPD). In order to...

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Detalles Bibliográficos
Autores principales: Shen, Ting, Pu, Jiali, Lai, Hsin-Yi, Xu, Lingjia, Si, Xiaoli, Yan, Yaping, Jiang, Yasi, Zhang, Baorong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6145881/
https://www.ncbi.nlm.nih.gov/pubmed/30232368
http://dx.doi.org/10.1038/s41598-018-32217-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6145881/
https://www.ncbi.nlm.nih.gov/pubmed/30232368
http://dx.doi.org/10.1038/s41598-018-32217-4

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