Rare homozygous PRKN exon 8 and 9 deletion in Malay familial early-onset Parkinson's disease
Ann Acad Med Singap
.
2021 Apr;50(4):353-355.
doi: 10.47102/annals-acadmedsg.2020508.
Authors
Yi Wen Tay
1
,
Jia Lun Lim
,
Ai Huey Tan
,
Azlina Ahmad Annuar
,
Shen Yang Lim
Affiliation
1
Department of Biomedical Science, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
PMID:
33990826
DOI:
10.47102/annals-acadmedsg.2020508
No abstract available
Publication types
Letter
MeSH terms
Age of Onset
Exons / genetics
Humans
Malaysia / epidemiology
Mutation
Parkinson Disease* / genetics