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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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| 主要な著者: | , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
The National Academy of Sciences
2002
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| 主題: | |
| オンライン･アクセス: | 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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