Novel calmodulin mutations associated with congenital arrhythmia susceptibility.

Makita N, Yagihara N, Crotti L, Johnson CN, Beckmann BM, Roh MS, Shigemizu D, Lichtner P, Ishikawa T, Aiba T, Homfray T, Behr ER, Klug D, Denjoy I, Mastantuono E, Theisen D, Tsunoda T, Satake W, Toda T, Nakagawa H, Tsuji Y, Tsuchiya T, Yamamoto H, Miyamoto Y, Endo N, Kimura A, Ozaki K, Motomura H, Suda K, Tanaka T, Schwartz PJ, Meitinger T, Kääb S, Guicheney P, Shimizu W, Bhuiyan ZA, Watanabe H, Chazin WJ, George AL
Circ Cardiovasc Genet. 2014 7 (4): 466-74

PMID: 24917665 · PMCID: PMC4140998 · DOI:10.1161/CIRCGENETICS.113.000459

MeSH Terms (22)

Adrenergic beta-Antagonists Adult Age of Onset Amino Acid Sequence Calcium Calmodulin Child Child, Preschool Electrocardiography Female Genetic Predisposition to Disease High-Throughput Nucleotide Sequencing Humans Infant Long QT Syndrome Male Molecular Sequence Data Mutation, Missense Pedigree Protein Binding Sequence Analysis, DNA Tachycardia, Ventricular

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