Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia

Circulation

Volumn 103, Issue 4, 2001, Pages 485-490

  Laitinen, Päivi J ^a,b,c,d,e   Brown, Kevin M ^a,b,c,d,e   Piippo, Kirsi ^a,b,c,d,e   Swan, Heikki ^a,b,c,d,e   Devaney, Joe M ^a,b,c,d,e   Brahmbhatt, Bhoomi ^a,b,c,d,e   Donarum, Elizabeth A ^a,b,c,d,e   Marino, Michael ^a,b,c,d,e   Tiso, Natascia ^a,b,c,d,e   Viitasalo, Matti ^a,b,c,d,e   Toivonen, Lauri ^a,b,c,d,e   Stephan, Dietrich A ^a,b,c,d,e   Kontula, Kimmo ^a,b,c,d,e  

^a UNIVERSITY OF HELSINKI   (Finland)

^b CHILDREN'S NATIONAL MEDICAL CENTER   (United States)

^c NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^d TRANSGENOMIC INC   (United States)

^e UNIVERSITY OF PADOVA   (Italy)

Author keywords

Genetics; Ryanodine receptor calcium release channel; Sarcoplastic reticulum; Tachycardia

Indexed keywords

RYANODINE RECEPTOR;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CALCIUM SIGNALING; CHROMOSOME 1Q; EXERCISE; FEMALE; GENE MUTATION; HEART VENTRICLE TACHYCARDIA; HUMAN; MALE; MISSENSE MUTATION; MORTALITY; MYOCARDIAL DISEASE; PHENOTYPE; PRIORITY JOURNAL;

EID: 0035969990     PISSN: 00097322     EISSN: None     Source Type: Journal    
DOI: 10.1161/01.CIR.103.4.485     Document Type: Article

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