Ann Child Neurol.  2019 Dec;27(4):149-151. 10.26815/acn.2019.00178.

Novel Mutation in KCNQ2 Causing Ohtahara Syndrome

Affiliations
  • 1Department of Pediatrics, Yeouido St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.
  • 2Department of Pediatrics, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea. iglee@catholic.ac.kr

Abstract

No abstract available.


MeSH Terms

Spasms, Infantile
Mutation
KCNQ2 Potassium Channel
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