Open AccessDoes a rare mutation in PTPRA contribute to the development of Parkinson’s disease in an Australian multi-incident family?
Author(s) -
Melissa A. Hill,
Steven R. Bentley,
Tara L. Walker,
George D. Mellick,
Stephen A. Wood,
Alex M. Sykes
Publication year - 2022
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0271499
Subject(s) - missense mutation , mutation , genetics , exome sequencing , biology , allele , penetrance , mutant , exome , lrrk2 , parkin , minor allele frequency , disease , phenotype , gene , medicine , allele frequency , parkinson's disease
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