Early-Onset Parkinson's Disease Caused by PLA2G6 Compound Heterozygous Mutation, a Case Report and Literature Review

PLA2G6 has been certified as a causative gene in patients with autosomal recessive early-onset Parkinson's disease (EOPD). We reported an EOPD case caused by PLA2G6 gene mutation, and performed neurological examination, genetic analysis, and multimodal neuroimaging to describe this phenotype. A...

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Detalles Bibliográficos
Autores principales: Shen, Ting, Hu, Jing, Jiang, Yasi, Zhao, Shuai, Lin, Caixiu, Yin, Xinzhen, Yan, Yaping, Pu, Jiali, Lai, Hsin-Yi, Zhang, Baorong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6712964/
https://www.ncbi.nlm.nih.gov/pubmed/31496990
http://dx.doi.org/10.3389/fneur.2019.00915

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6712964/
https://www.ncbi.nlm.nih.gov/pubmed/31496990
http://dx.doi.org/10.3389/fneur.2019.00915

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