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Heart Rhythm. 2015 Feb;12(2):419-22. doi: 10.1016/j.hrthm.2014.10.035. Epub 2014 Oct 31.

CALM3 mutation associated with long QT syndrome.

Author information

1
Department of Molecular Pharmacology and Experimental Therapeutics, Windland Smith Rice Sudden Death Genomics Laboratory.
2
Department of Molecular Pharmacology and Experimental Therapeutics, Windland Smith Rice Sudden Death Genomics Laboratory; Center for Clinical and Translational Science; Mayo Graduate School, Mayo Clinic, Rochester, Minnesota.
3
Primary Children's Hospital, Salt Lake City, Utah.
4
Department of Molecular Pharmacology and Experimental Therapeutics, Windland Smith Rice Sudden Death Genomics Laboratory; Division of Cardiovascular Diseases, Department of Medicine; Division of Pediatric Cardiology, Department of Pediatrics, Mayo Clinic, Rochester, Minnesota. Electronic address: ackerman.michael@mayo.edu.

KEYWORDS:

Arrhythmia; CALM3; Calcium channel inactivation; Calmodulin; Genetics; Long QT syndrome

Comment in

PMID:
25460178
PMCID:
PMC4907373
DOI:
10.1016/j.hrthm.2014.10.035
[Indexed for MEDLINE]
Free PMC Article

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