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Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias.

Mutations in the delayed rectifier K+ channel subunit KvLQT1 have been identified as responsible for both Romano-Ward (RW) and Jervell and Lange-Nielsen (JLN) inherited long QT syndromes. We report the molecular cloning of a human KvLQT1 isoform that is expressed in several human tissues including h...

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Bibliografiske detaljer
Main Authors: Chouabe, C, Neyroud, N, Guicheney, P, Lazdunski, M, Romey, G, Barhanin, J
Format: Artigo
Sprog:Inglês
Udgivet: 1997
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1170178/
https://ncbi.nlm.nih.gov/pubmed/9312006
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/emboj/16.17.5472
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