Channelopathies: Kir2.1 mutations jeopardize many cell functions

H. J. Jongsma; R. Wilders

doi:https://doi.org/10.1016/S0960-9822(01)00437-7

Channelopathies: Kir2.1 mutations jeopardize many cell functions

H. J. Jongsma, R. Wilders

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Research output: Contribution to journal › Article › Academic › peer-review

52 Citations (Scopus)

Abstract

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

Original language	English
Pages (from-to)	R747-R750
Journal	Current biology
Volume	11
Issue number	18
DOIs	https://doi.org/10.1016/S0960-9822(01)00437-7
Publication status	Published - 2001

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https://doi.org/10.1016/S0960-9822(01)00437-7

Cite this

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title = "Channelopathies: Kir2.1 mutations jeopardize many cell functions",

abstract = "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",

author = "Jongsma, {H. J.} and R. Wilders",

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AU - Wilders, R.

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AB - 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

U2 - https://doi.org/10.1016/S0960-9822(01)00437-7

DO - https://doi.org/10.1016/S0960-9822(01)00437-7

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C2 - 11566119

SN - 0960-9822

VL - 11

SP - R747-R750

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JF - Current biology

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