Channelopathies: Kir2.1 mutations jeopardize many cell functions

نویسندگان

  • Habo J Jongsma
  • Ronald Wilders
چکیده

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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عنوان ژورنال:
  • Current Biology

دوره 11  شماره 

صفحات  -

تاریخ انتشار 2001