Article

Overexpressing PLA2G6 mutations cause symptoms of young–onset dystonia–parkinsonism type 14

2020-12-01

Abstract excerpt

<title>Abstract</title> <p>Background: Parkinson’s disease (PD) is the most common neurodegenerative motor disorder, which is currently incurable. Mutations in many genes have been demonstrated to be the primary risk factors associated with the familial or idiopathic PD; however, the mechanisms underlying these genetic mutations resulting in parkinsonism remains unclear. Phospholipase A2 group VI (PLA2G6) has bee...

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Literature Corpus work: 7fd1a4da-2f82-519e-b2c5-5c8e0a037252
DOI: 10.21203/rs.3.rs-25963/v2

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Overexpressing PLA2G6 mutations cause symptoms of young–onset dystonia–parkinsonism type 14DOI 10.21203/rs.3.rs-25963/v2Read

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