Search for cardiac calcium cycling gene mutations in familial ventricular arrhythmias resembling catecholaminergic polymorphic ventricular tachycardia

BMC Medical Genetics

Volumn 10, Issue , 2009, Pages

  Marjamaa, Annukka ^a   Laitinen Forsblom, Päivi ^a   Lahtinen, Annukka M ^a   Viitasalo, Matti ^a   Toivonen, Lauri ^a   Kontula, Kimmo ^a   Swan, Heikki ^a  

^a UNIVERSITY OF HELSINKI   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

CALSTABIN; CARRIER PROTEIN; PROTEIN ATP2A2; PROTEIN SLC8A1; RYANODINE RECEPTOR 2; UNCLASSIFIED DRUG; CATECHOLAMINE; RYANODINE RECEPTOR;

ADOLESCENT; ADULT; ARTICLE; CALCIUM TRANSPORT; CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; ECHOCARDIOGRAPHY; EXERCISE TEST; FAMILY HISTORY; FEMALE; GENE DELETION; GENE MUTATION; GENE SEQUENCE; GENETIC VARIABILITY; HEART VENTRICLE EXTRASYSTOLE; HUMAN; MALE; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PHENOTYPE; RISK FACTOR; ELECTROCARDIOGRAPHY; EXON; GENETICS; HEART VENTRICLE TACHYCARDIA; MIDDLE AGED; PRESCHOOL CHILD;

SYNCOPE;

ADOLESCENT; ADULT; CATECHOLAMINES; CHILD; CHILD, PRESCHOOL; ELECTROCARDIOGRAPHY; EXONS; FEMALE; HUMANS; MALE; MIDDLE AGED; MUTATION, MISSENSE; PHENOTYPE; RYANODINE RECEPTOR CALCIUM RELEASE CHANNEL; TACHYCARDIA, VENTRICULAR; VENTRICULAR PREMATURE COMPLEXES; YOUNG ADULT;

EID: 64549091384     PISSN: None     EISSN: 14712350     Source Type: Journal    
DOI: 10.1186/1471-2350-10-12     Document Type: Article

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