Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death

American Journal of Human Genetics

Volumn 91, Issue 4, 2012, Pages 703-712

  Nyegaard, Mette ^a   Overgaard, Michael T ^b   Sondergaard, Mads T ^b   Vranas, Marta ^a   Behr, Elijah R ^c   Hildebrandt, Lasse L ^b   Lund, Jacob ^b   Hedley, Paula L ^d,e   Camm, A John ^c   Wettrell, Göran ^f   Fosdal, Inger ^g   Christiansen, Michael ^d   Borglum, Anders D ^a  

^a AARHUS UNIVERSITY   (Denmark)

^b AALBORG UNIVERSITY   (Denmark)

^c ST GEORGE'S UNIVERSITY OF LONDON   (United Kingdom)

^d STATENS SERUM INSTITUT   (Denmark)

^e UNIVERSITY OF STELLENBOSCH   (South Africa)

^f LUND UNIVERSITY HOSPITAL   (Sweden)

^g Visby Hospital   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CALMODULIN GENE; CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA; CHROMOSOME 14Q; ELECTROCARDIOGRAPHY; GENE; GENE LOCUS; GENE MAPPING; GENE SEQUENCE; HUMAN; MISSENSE MUTATION; PEDIGREE; PRIORITY JOURNAL; RYR2 GENE; SUDDEN DEATH;

ADOLESCENT; ADULT; AMINO ACID SEQUENCE; ARRHYTHMIAS, CARDIAC; CALCIUM CHANNELS; CALMODULIN; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 14; DEATH, SUDDEN, CARDIAC; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HETEROZYGOTE; HUMANS; MALE; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; RYANODINE RECEPTOR CALCIUM RELEASE CHANNEL; SYNCOPE; TACHYCARDIA, VENTRICULAR; YOUNG ADULT;

EID: 84867242998     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2012.08.015     Document Type: Article

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