Title : A novel mutation associated with Jervell and Lange-Nielsen syndrome in a Japanese family.

Pub. Date : 2008 May

PMID : 18441444






1 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 The syndrome is caused by homozygous or compound heterozygous mutations in genes KCNQ1 and KCNE1, which are responsible for encoding the delayed rectifier repolarizing current, I(Ks). Potassium potassium voltage-gated channel subfamily E regulatory subunit 1 Homo sapiens