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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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Hlavní autoři: Smith, Jarrod, Vanoye, Carlos G., George, Alfred L., Meiler, Jens, Sanders, Charles R.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2007
Témata:
On-line přístup: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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