- The First Korean Case of KCNQ2 Mutation in a Family with Benign Familial Neonatal Convulsions
-
Yum MS, Ko TS, Yoo HW
- KMID: 1779270
- J Korean Med Sci.
- 2010 Feb;25(2):324-326.
- doi: 10.3346/jkms.2010.25.2.324
Neonatal seizures represent a heterogeneous group of disorders with vastly different etiologies and outcomes. Benign familial neonatal convulsions (BFNC) are a distinctive epileptic syndrome of autosomal dominant inheritance with a... -
- CITED
-
- Close
- SHARE
-
- Close
- Novel Mutation in KCNQ2 Causing Ohtahara Syndrome
-
Yoon DH, Moon JU, Lee JY, Lee IG
- KMID: 2470592
- Ann Child Neurol.
- 2019 Dec;27(4):149-151.
- doi: 10.26815/acn.2019.00178
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- Long QT Syndrome: a Korean Single Center Study
-
Lee YS, Kwon BS, Kim GB, Oh SI, Bae EJ, Park SS, Noh CI
- KMID: 1777681
- J Korean Med Sci.
- 2013 Oct;28(10):1454-1460.
- doi: 10.3346/jkms.2013.28.10.1454
The long QT syndrome (LQTS) is a rare hereditary disorder in which affected individuals have a possibility of ventricular tachyarrhythmia and sudden cardiac death. We investigated 62 LQTS (QTc >... -
- CITED
-
- Close
- SHARE
-
- Close
