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Case report: A Chinese child with Andersen–Tawil syndrome due to a de novo KCNJ2 mutation
Journal of the Neurological Sciences, 2015Hai-Yan Zhou, Tian Wang, Jun-Yi Shen
exaly
KCNJ2mutation in intractable ventricular arrhythmia with Andersen's syndrome
Pediatrics International, 2005exaly
Function, subcellular localization and assembly of a novel mutation of KCNJ2 in Andersen's syndrome
Journal of Molecular and Cellular Cardiology, 2003exaly

