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 comp...

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Autors principals:	Ting Shen, Jing Hu, Yasi Jiang, Shuai Zhao, Caixiu Lin, Xinzhen Yin, Yaping Yan, Jiali Pu, Hsin-Yi Lai, Baorong Zhang
Format:	Artigo
Idioma:	Inglês
Publicat:	Frontiers Media S.A. 2019-08-01
Col·lecció:	Frontiers in Neurology
Matèries:	Parkinson's disease early-onset PLA2G6 genetic analysis neuroimaging
Accés en línia:	https://www.frontiersin.org/article/10.3389/fneur.2019.00915/full
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