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Article

The Genetic Architecture of Parkinson's Disease in Morocco: Highlighting a Predominance of Mendelian Genes.

Neuro-degenerative diseases - 1 Jan 2025

Bouhouche Ahmed, Tibar Houyam, Regragui Wafa

Abstract excerpt

<p>Background: Parkinson's disease (PD), although widely heterogeneous and manifesting with numerous motor and non-motor symptoms, presents clinically as a single entity worldwide. Its genetic causes are also heterogeneous and include highly penetrant variants in a single gene representing rare monogenic forms, and rare or common variants conferring a relative disease risk representing more frequent multigenic...

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Identifiers

PMID: 40393443
DOI: 10.1159/000546424
PMCID: PMC12178584

Genes

MAPT
PINK1
POLG
PRKN
VPS13C

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

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