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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Bibliografske podrobnosti
izdano v:Front Neurol
Main Authors: Shen, Ting, Hu, Jing, Jiang, Yasi, Zhao, Shuai, Lin, Caixiu, Yin, Xinzhen, Yan, Yaping, Pu, Jiali, Lai, Hsin-Yi, Zhang, Baorong
Format: Artigo
Jezik:Inglês
Izdano: Frontiers Media S.A. 2019
Teme:
Neurology
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6712964/
https://ncbi.nlm.nih.gov/pubmed/31496990
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2019.00915
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