Open AccessHeterozygous PRKN mutations are common but do not increase the risk of Parkinson’s disease
Author(s) -
William Zhu,
Xiaoping Huang,
Esther Yoon,
Sara BandrésCiga,
Cornelis Blauwendraat,
Kimberly J Billingsley,
Joshua H. Cade,
Beverly P Wu,
Victoria H. Williams,
Alice B. Schindler,
Janet Brooks,
J. Raphael Gibbs,
Dena Hernández,
Debra Ehrlich,
Andrew Singleton,
Derek P. Narendra
Publication year - 2021
Publication title -
brain
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.142
H-Index - 336
eISSN - 1460-2156
pISSN - 0006-8950
DOI - 10.1093/brain/awab456
Subject(s) - genotyping , genetics , copy number variation , biology , biobank , exome sequencing , single nucleotide polymorphism , population , 1000 genomes project , cohort , disease , genotype , mutation , medicine , genome , gene , environmental health
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