• Vol. 50 No. 4, 353–355
  • 15 April 2021

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



Download PDF

Little is known about the genetics of Parkinson’s disease (PD) in Southeast Asian populations.1 We extended knowledge of the Southeast Asian monogenic PD landscape by describing a Malaysian Malay family with early-onset PD (EOPD), defined as onset at <50 years of age and a rarely reported homozygous PRKN exon 8 and 9 deletion.

This article is available only as a PDF. Please click on “Download PDF” on top to view the full article.