TY  - GEN
AU  - Saenen,J B
AU  - Paulussen,A D C
AU  - Jongbloed,R J
AU  - Marcelis,C L
AU  - Gilissen,R A H J
AU  - Aerssens,J
AU  - Snyders,D J
AU  - Raes,A L
TI  - A single hERG mutation underlying a spectrum of acquired and congenital long QT syndrome phenotypes
SN  - 0022-2828
PY  - 2008///0225
KW  - Aged
KW  - Amino Acid Sequence
KW  - Amino Acid Substitution
KW  - genetics
KW  - Base Sequence
KW  - Canada
KW  - Cell Line
KW  - Ether-A-Go-Go Potassium Channels
KW  - Female
KW  - Genetic Diseases, Inborn
KW  - Humans
KW  - Long QT Syndrome
KW  - Netherlands
KW  - Pedigree
KW  - Phenotype
KW  - Point Mutation
KW  - White People
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.yjmcc.2007.04.012
ER  -