• 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

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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.

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