Results 181 to 190 of about 6,365 (192)
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Functional analysis of a double-point mutation in the KCNJ2 gene identified in a family with Andersen-Tawil syndrome

Journal of the Neurological Sciences, 2019
Shinobu Fukumura   +2 more
exaly  

Electrocardiographic Features in Andersen-Tawil Syndrome Patients With KCNJ2 Mutations

Circulation, 2005
Li Zhang   +2 more
exaly  

Novel mechanism of KCNJ2-related short QT syndrome

2011
Ruan Y.   +9 more
openaire   +1 more source

Long-Term Arrhythmic Outcomes of KCNJ2 Variant Carriers in Japan

Circulation: Genomic and Precision Medicine
Koichi Kato   +11 more
openaire   +1 more source

Case report: A Chinese child with Andersen–Tawil syndrome due to a de novo KCNJ2 mutation

Journal of the Neurological Sciences, 2015
Hai-Yan Zhou, Tian Wang, Jun-Yi Shen
exaly  

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