TY  - GEN
AU  - Crotti,Lia
AU  - Spazzolini,Carla
AU  - Schwartz,Peter J
AU  - Shimizu,Wataru
AU  - Denjoy,Isabelle
AU  - Schulze-Bahr,Eric
AU  - Zaklyazminskaya,Elena V
AU  - Swan,Heikki
AU  - Ackerman,Michael J
AU  - Moss,Arthur J
AU  - Wilde,Arthur A M
AU  - Horie,Minoru
AU  - Brink,Paul A
AU  - Insolia,Roberto
AU  - De Ferrari,Gaetano M
AU  - Crimi,Gabriele
TI  - The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratification
SN  - 1524-4539
PY  - 2007///1212
KW  - Adolescent
KW  - Adult
KW  - Child
KW  - Child, Preschool
KW  - Ethnicity
KW  - genetics
KW  - Female
KW  - Humans
KW  - International Cooperation
KW  - KCNQ1 Potassium Channel
KW  - Long QT Syndrome
KW  - Male
KW  - Middle Aged
KW  - Mutation
KW  - Risk Factors
KW  - Severity of Illness Index
N1  - Publication Type: Comparative Study; Journal Article; Multicenter Study; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1161/CIRCULATIONAHA.107.726950
ER  -