Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosis

Background: Mutations in the PRRT2 gene have been identified as the major cause of benign http://t.co/JjXuGN3IV5

#neurology Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infa... http://t.co/PTeyVxuyaW