Heteromerization of Kir2.x potassium channels contributes to the phenotype of Andersen's syndrome

Andersen's syndrome, an autosomal dominant disorder related to mutations of the potassium channel Kir2.1, is characterized by cardiac arrhythmias, periodic paralysis, and dysmorphic bone structure. The aim of our study was to find out whether heteromerization of Kir2.1 channels with wild-type K...

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Bibliographic Details
Main Authors: Preisig-Müller, Regina, Schlichthörl, Günter, Goerge, Tobias, Heinen, Steffen, Brüggemann, Andrea, Rajan, Sindhu, Derst, Christian, Veh, Rüdiger W., Daut, Jürgen
Format: Artigo
Language:Inglês
Published: The National Academy of Sciences 2002
Subjects:
Biological Sciences
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC124349/
https://ncbi.nlm.nih.gov/pubmed/12032359
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.102609499
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