|
The Kir2.1 inward-rectifier potassium ion channel is encoded by the gene. == Clinical significance == A defect in this gene is associated with Andersen-Tawil syndrome. A mutation in the KCNJ2 gene has also been shown to cause short QT syndrome. 抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「Kir2.1」の詳細全文を読む スポンサード リンク
|