Novel Calmodulin Mutations Associated With Congenital Arrhythmia Susceptibility - Makita, Naomasa; Yagihara, Nobue; Crotti, Lia; Johnson, Christopher N.; Beckmann, Britt-Maria; Roh, Michelle S.; Shigemizu, Daichi; Lichtner, Peter; Ishikawa, Taisuke; Aiba, Takeshi; Homfray, Tessa; Behr, Elijah R.; et al. (Circulation. Cardiovascular genetics, 2014)
Keywords: Adrenergic beta-Antagonists - therapeutic use; Adult; Age of Onset; Amino Acid Sequence; Calcium - chemistry; Calcium - metabolism; Calmodulin - genetics; Calmodulin - metabolism; Child; Child, Preschool; Electrocardiography; Female; Genetic Predisposition to Disease; High-Throughput Nucleotide Sequencing; Humans; Infant; Long QT Syndrome - drug therapy; Long QT Syndrome - genetics; Long QT Syndrome - pathology; Male; Molecular Sequence Data; Mutation, Missense; Pedigree; Protein Binding; Sequence Analysis, DNA; Tachycardia, Ventricular - drug therapy; Tachycardia, Ventricular - genetics; Tachycardia, Ventricular - pathology; long QT syndrome; calmodulin