Clinical and genetic characteristics of PLA2G6-parkinsonism in southwest China and a review of heterogeneity of phenotype and genotype between Asian and Caucasian patients

Background: Biallelic PLA2G6 mutations were identified as responsible for autosomal-recessive early-onset parkinsonism, while PLA2G6-mutant parkinsonism has a huge clinical heterogeneity.
Source: Parkinsonism and Related Disorders - Category: Neurology Authors: Source Type: research