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Four novel rare mutations of PLA2G6 in Chinese population with Parkinson's disease

✍ Scribed by Ya-Xing Gui; Zhong-Ping Xu; Wen-Lv; Hong-mei Liu; Jin-Jia Zhao; Xing-Yue Hu


Book ID
119343106
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
702 KB
Volume
19
Category
Article
ISSN
1353-8020

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## Abstract Mutations of __PLA2G6__ gene have been lately proposed to be the causative gene for PARK14 in patients with autosomal recessive young‐onset parkinsonism (YOPD). The role of __PLA2G6__ mutations as a risk factor for Parkinson's disease is not clear. To study the __PLA2G6__ mutations in P