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Updated: Jul 28, 2026

15:28
Mutagenesis and Functional Analysis of Ion Channels Heterologously Expressed in Mammalian Cells
Published on: October 1, 2010
Channelopathies: Kir2.1 mutations jeopardize many cell functions
1Department of Medical Physiology, University Medical Center Utrecht, PO Box 85060, 3508 AB Utrecht, The Netherlands. h.j.jongsma@med.uu.nl
Current Biology : CB
|September 22, 2001
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.
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