Four novel rare mutations of PLA2G6 in Chinese population with Parkinson's disease.

Abstract excerpt

BACKGROUND: Mutations in the phospholipase A2 Group 6 (PLA2G6) gene have been identified in autosomal recessive neurodegenerative diseases classified as infantile neuroaxonal dystrophy and neurodegeneration with brain iron accumulation. Recently, PLA2G6 was also reported as the causative gene for early-onset PARK14-linked dystonia-parkinsonism. METHODS/RESULTS: To address whether PLA2G6 mutations are also an...

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