TY  - GEN
AU  - Mohler,Peter J
AU  - Le Scouarnec,Solena
AU  - Denjoy,Isabelle
AU  - Lowe,John S
AU  - Guicheney,Pascale
AU  - Caron,Lise
AU  - Driskell,Iwona M
AU  - Schott,Jean-Jacques
AU  - Norris,Kris
AU  - Leenhardt,Antoine
AU  - Kim,Richard B
AU  - Escande,Denis
AU  - Roden,Dan M
TI  - Defining the cellular phenotype of "ankyrin-B syndrome" variants: human ANK2 variants associated with clinical phenotypes display a spectrum of activities in cardiomyocytes
SN  - 1524-4539
PY  - 2007///0220
KW  - Aged
KW  - Animals
KW  - Ankyrins
KW  - genetics
KW  - Arrhythmias, Cardiac
KW  - chemically induced
KW  - Asian People
KW  - Black People
KW  - Cytoskeleton
KW  - physiology
KW  - Female
KW  - Genetic Variation
KW  - Genotype
KW  - Humans
KW  - Ion Channels
KW  - Long QT Syndrome
KW  - Male
KW  - Mexican Americans
KW  - Mice
KW  - Mice, Inbred C57BL
KW  - Middle Aged
KW  - Myocytes, Cardiac
KW  - cytology
KW  - Phenotype
KW  - Tachycardia, Ventricular
KW  - Torsades de Pointes
KW  - White People
N1  - Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1161/CIRCULATIONAHA.106.656512
ER  -