A single hERG mutation underlying a spectrum of acquired and congenital long QT syndrome phenotypes.

Saenen, J B

A single hERG mutation underlying a spectrum of acquired and congenital long QT syndrome phenotypes. [electronic resource] - Journal of molecular and cellular cardiology Jul 2007 - 63-72 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

0022-2828

10.1016/j.yjmcc.2007.04.012 doi


Aged
Amino Acid Sequence
Amino Acid Substitution--genetics
Base Sequence
Canada
Cell Line
Ether-A-Go-Go Potassium Channels--genetics
Female
Genetic Diseases, Inborn
Humans
Long QT Syndrome--genetics
Netherlands
Pedigree
Phenotype
Point Mutation
White People