Genetic analysis of <ce:italic>PRRT2</ce:italic> for benign infantile epilepsy, infantile convulsions with choreoathetosis syndrome, and benign convulsions with mild gastroenteritis

@article{Ishii2013GeneticAO,
  title={Genetic analysis of <ce:italic>PRRT2</ce:italic> for benign infantile epilepsy, infantile convulsions with choreoathetosis syndrome, and benign convulsions with mild gastroenteritis},
  author={A Ishii and Sawa Yasumoto and Yukiko Ihara and Takahito Inoue and Shinichi Hirose},
  journal={Brain and Development},
  year={2013},
  volume={35},
  pages={524-530}
}
PURPOSE PRRT2 mutations were recently identified in benign familial infantile epilepsy (BFIE) and infantile convulsions with paroxysmal choreoathetosis (ICCA) but no abnormalities have so far been identified in their phenotypically similar seizure disorder of benign convulsions with mild gastroenteritis (CwG), while mutations in KCNQ2 and KCNQ3 have been recognized in benign familial neonatal epilepsy (BFNE). The aim of this study was to identify PRRT2 mutations in infantile convulsions in… CONTINUE READING
Recent Discussions
This paper has been referenced on Twitter 2 times over the past 90 days. VIEW TWEETS

Similar Papers

Loading similar papers…