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Rare homozygous PRKN exon 8 and 9 deletion in Malay familial early-onset Parkinson's disease

Tay YW 1 , Lim JL , Tan AH , Annuar AA , Lim SY

Affiliations 

  • 1 Department of Biomedical Science, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia
Ann Acad Med Singap, 2021 04;50(4):353-355.
PMID: 33990826 DOI: 10.47102/annals-acadmedsg.2020508

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