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

相似書籍

• PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome
  由: Heron, Sarah E., et al.
  出版: (2012)
• A case report of PRRT2 mutation-associated familial convulsions with paroxysmal choreoathetosis syndrome
  由: M. A. Trishchynska, et al.
  出版: (2019-12-01)
• Novel PRRT2 gene variants identified in paroxysmal kinesigenic dyskinesia and benign familial infantile epilepsy in Chinese families
  由: He, Jialinzi, et al.
  出版: (2021)
• Genetic analysis of benign familial epilepsies in the first year of life in a Chinese cohort
  由: Zeng, Qi, et al.
  出版: (2017)
• PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine
  由: Cloarec, Robin, et al.
  出版: (2012)