期刊： MOVEMENT DISORDERS, 2020; 35 (4)
Background Heterozygous mutations in the glucocerebrosidase gene (GBA) have been shown to be an important genetic risk factor for Parkinson's disease ......
期刊： MOVEMENT DISORDERS, 2020; 35 (4)
Background Biallelic mutations in the MYORG gene were first identified as the cause of recessively inherited primary familial brain calcification. Int......
期刊： MOVEMENT DISORDERS, 2020; 35 (8)
Background Paroxysmal kinesigenic dyskinesia is a spectrum of involuntary dyskinetic disorders with high clinical and genetic heterogeneity. Mutations......
期刊： MOVEMENT DISORDERS, 2020; 35 (8)
Objective Accurate diagnosis is particularly challenging in Parkinson's disease (PD), multiple system atrophy (MSAp), and progressive supranuclear pal......
期刊： MOVEMENT DISORDERS, 2020; 35 (7)
Background Hemizygous mutations in GRIA3 encoding the GluA3 subunit of the amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor are known to be......
