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Preparation, Functional Characterization, and NMR Studies of Human KCNE1, a Voltage-Gated Potassium Channel Accessory Subunit Associated With Deafness and Long QT Syndrome

KCNE1, also known as minK, is a member of the KCNE family of membrane proteins that modulate the function of KCNQ1 and certain other voltage-gated potassium channels (K(V)). Mutations in human KCNE1 cause congenital deafness and congenital long QT syndrome, an inherited predisposition to potentially...

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Detalhes bibliográficos
Main Authors: Tian, Changlin, Vanoye, Carlos G., Kang, Congbao, Welch, Richard C., Kim, Hak Jun, George, Alfred L., Sanders, Charles R.
Formato: Artigo
Idioma:Inglês
Publicado em: 2007
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2565491/
https://ncbi.nlm.nih.gov/pubmed/17892302
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/bi700705j
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