- Paroxysmal kinesigenic dyskinesia–like phenotype in multiple sclerosis
Roxana Pop et al, 2017, Mult Scler CrossRef - PRRT2 mutations in a cohort of Chinese families with paroxysmal kinesigenic dyskinesia and genotype–phenotype correlation reanalysis in literatures
Guohua Zhao et al, 2018, International Journal of Neuroscience CrossRef -
A novel
PRRT2
pathogenic variant in a family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures
Jacqueline G. Lu et al, 2018, Cold Spring Harb Mol Case Stud CrossRef - Diagnostic outcomes for genetic testing of 70 genes in 8565 patients with epilepsy and neurodevelopmental disorders
Amanda S. Lindy et al, 2018, Epilepsia CrossRef - Diagnosis and Management of Dystonia
Vicki Shanker et al, 2016, CONTINUUM: Lifelong Learning in Neurology CrossRef - Case report: Homozygous PRRT2 mutation in ICCA Egyptian family with reduced penetrance
Nirmeen A. Kishk et al, 2017, Meta Gene CrossRef