Alanine

potassium inwardly rectifying channel subfamily J member 2 ; Homo sapiens







2 Article(s)
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1 28188270 Dual Mechanism for Inhibition of Inwardly Rectifying Kir2.x Channels by Quinidine Involving Direct Pore Block and PIP2-interference. 2017 May 1
2 15276028 Loss-of-function mutations of the K(+) channel gene KCNJ2 constitute a rare cause of long QT syndrome. 2004 Aug 1