Rare homozygous PRKN exon 8 and 9 deletion in Malay familial early-onset Parkinson's disease
- PMID: 33990826
- DOI: 10.47102/annals-acadmedsg.2020508
Rare homozygous PRKN exon 8 and 9 deletion in Malay familial early-onset Parkinson's disease
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