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Structural Models for the KCNQ1 Voltage-Gated Potassium Channel
Mutations in the human voltage-gated potassium channel KCNQ1 are associated with predisposition to deafness and various cardiac arrhythmia syndromes including congenital long QT syndrome, familial atrial fibrillation, and sudden infant death syndrome. In this work 3-D structural models were develope...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2565492/ https://ncbi.nlm.nih.gov/pubmed/17999538 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/bi701597s |
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