Genetic variants in SCN5A promoter are associated with arrhythmia phenotype severity in patients with heterozygous loss-of-function mutation
Park, Ji Kwon, Martin, Lisa J., Zhang, Xue, Jegga, Anil G., Benson, D. WoodrowVolume:
9
Language:
english
Journal:
Heart Rhythm
DOI:
10.1016/j.hrthm.2012.02.023
Date:
July, 2012
File:
PDF, 1.79 MB
english, 2012