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Article

Autophagy and Its Association with Genetic Mutations in Parkinson Disease.

Medical science monitor : international medical journal of experimental and clinical research - 11 Nov 2022

Erekat Nour S

Abstract excerpt

Parkinson disease is the second most common neurodegenerative disorder, affecting 0.1-0.2% of the general population. It is a progressive debilitating disorder caused by degeneration of dopaminergic neurons in the substantia nigra pars compacta. It is characterized by motor and non-motor symptoms. Parkinson disease can be caused by mutations in genes that encode proteins involved in the autophagic process,...

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Identifiers

PMID: 36366737
DOI: 10.12659/MSM.938519
PMCID: PMC9664771

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