Four novel rare mutations of PLA2G6 in Chinese population with Parkinson's disease
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Geriatrics and Gerontology,Neurology
Reference29 articles.
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2. Parkinson's disease;Samii;Lancet,2004
3. PLA2G6 mutation underlies infantile neuroaxonal dystrophy;Khateeb;Am J Hum Genet,2006
4. PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron;Morgan;Nat Genet,2006
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2. Effect of PLA2G6 and SMPD1 Variants on the Lipid Metabolism in the Cerebrospinal Fluid of Patients with Parkinson's Disease: A Non-targeted Lipidomics Study;Neurology and Therapy;2023-09-14
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5. Case Report: A case of PLA2G6 gene-related early-onset Parkinson's disease and review of literature;Frontiers in Neuroscience;2022-12-09
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