Heteromerization of Kir2.x Potassium Channels Contributes to the Phenotype of Andersen's Syndrome
Heteromerization of Kir2.x Potassium Channels Contributes to the Phenotype of Andersen's Syndrome
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United States: National Academy of Sciences
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Language
English
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United States: National Academy of Sciences
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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 Kir2.2 and Kir2.3 channels contributes to the phenotype...
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Full title
Heteromerization of Kir2.x Potassium Channels Contributes to the Phenotype of Andersen's Syndrome
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TN_cdi_proquest_miscellaneous_18327874
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_18327874
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ISSN
0027-8424
E-ISSN
1091-6490
DOI
10.1073/pnas.102609499
