Channelopathies: Kir2.1 mutations jeopardize many cell functions
Channelopathies: Kir2.1 mutations jeopardize many cell functions
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DOI：
10.1016/s0960-9822(01)00437-7
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发表时间：
2001-09-18
期刊：
影响因子：
9.2
通讯作者：
Wilders, R
中科院分区：
文献类型：
--
作者：
Jongsma, HJ;Wilders, R
安德森综合征是由钾通道Kir2.1突变引起的，Kir2.1是静息膜电位的主要决定因素。这种疾病的临床特征说明了稳定的静息膜电位对许多细胞功能的重要性。
Andersen's syndrome is caused by mutations in the potassium channel Kir2.1, a major determinant of resting membrane potential. The clinical features of this disease illustrate the importance of a stable resting membrane potential for many cell functions.