TY  - GEN
AU  - Behr,Elijah R
AU  - Savio-Galimberti,Eleonora
AU  - Barc,Julien
AU  - Holst,Anders G
AU  - Petropoulou,Evmorfia
AU  - Prins,Bram P
AU  - Jabbari,Javad
AU  - Torchio,Margherita
AU  - Berthet,Myriam
AU  - Mizusawa,Yuka
AU  - Yang,Tao
AU  - Nannenberg,Eline A
AU  - Dagradi,Federica
AU  - Weeke,Peter
AU  - Bastiaenan,Rachel
AU  - Ackerman,Michael J
AU  - Haunso,Stig
AU  - Leenhardt,Antoine
AU  - Kääb,Stefan
AU  - Probst,Vincent
AU  - Redon,Richard
AU  - Sharma,Sanjay
AU  - Wilde,Arthur
AU  - Tfelt-Hansen,Jacob
AU  - Schwartz,Peter
AU  - Roden,Dan M
AU  - Bezzina,Connie R
AU  - Olesen,Morten
AU  - Darbar,Dawood
AU  - Guicheney,Pascale
AU  - Crotti,Lia
AU  - Jamshidi,Yalda
TI  - Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study
SN  - 1755-3245
PY  - 2016///0210
KW  - Action Potentials
KW  - Adult
KW  - Aged
KW  - Brugada Syndrome
KW  - diagnosis
KW  - Case-Control Studies
KW  - Cell Line
KW  - Computational Biology
KW  - DNA Mutational Analysis
KW  - Databases, Genetic
KW  - Europe
KW  - Female
KW  - Gene Frequency
KW  - Genetic Association Studies
KW  - Genetic Predisposition to Disease
KW  - Heredity
KW  - Humans
KW  - Male
KW  - Middle Aged
KW  - NAV1.8 Voltage-Gated Sodium Channel
KW  - genetics
KW  - Odds Ratio
KW  - Pedigree
KW  - Phenotype
KW  - Polymorphism, Single Nucleotide
KW  - Risk Factors
KW  - Saudi Arabia
KW  - Transfection
KW  - United States
N1  - Publication Type: Journal Article; Multicenter Study; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1093/cvr/cvv042
ER  -