Associated Papers
Genetic and phenotypic analyses of PRRT2 positive and negative paroxysmal kinesigenic dyskinesia.
Zhang Y et al.
Therapeutic Advances in Neurological Disorders, 2024
Three siblings with self-limited familial infantile epilepsy with PRRT2 mutation: A case series.
Iwanami N et al.
Sage Open Medical Case Reports, 2024
The Genotype and Phenotype of Proline-Rich Transmembrane Protein 2 Associated Disorders in Chinese Children.
Luo HY et al.
Frontiers in Pediatrics, 2021
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