Linkage of Benign Familial Infantile Convulsions to Chromosome 16p12-q12 Suggests Allelism to the Infantile Convulsions and Choreoathetosis Syndrome

Podobne zapisy

• PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine
  od: Cloarec, Robin, i wsp.
  Wydane: (2012)
• Familial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16.
  od: Szepetowski, P, i wsp.
  Wydane: (1997)
• PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome
  od: Heron, Sarah E., i wsp.
  Wydane: (2012)
• Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosis
  od: Yang, Xiaoling, i wsp.
  Wydane: (2013)
• Mutations in the novel protein PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions
  od: Lee, Hsien-Yang, i wsp.
  Wydane: (2011)