Cardiac myosin-binding protein C gene mutation expressed as hypertrophic cardiomyopathy and left ventricular noncompaction within two families: Insights from cardiac magnetic resonance in clinical screening: Camuglia MYBPC3 gene mutation and MRI

International Journal of Cardiology

Volumn 168, Issue 3, 2013, Pages 2950-2952

  Camuglia, Anthony C ^a,b   Younger, John F ^a,b   McGaughran, Julie ^a,b   Lo, Ada ^a   Atherton, John J ^a,b  

^a ROYAL BRISBANE AND WOMEN'S HOSPITAL   (Australia)

^b UNIVERSITY OF QUEENSLAND   (Australia)

Author keywords

Cardiomyopathy; Genetic heart disease; Magnetic resonance imaging; Screening

Indexed keywords

CARRIER PROTEIN; MYOSIN-BINDING PROTEIN C;

CARDIAC IMAGING; CARDIOMYOPATHY, HYPERTROPHIC; CASE REPORT; FEMALE; GENETICS; HUMAN; ISOLATED NONCOMPACTION OF THE VENTRICULAR MYOCARDIUM; MIDDLE AGED; MUTATION; NUCLEAR MAGNETIC RESONANCE IMAGING; YOUNG ADULT;

CARDIAC IMAGING TECHNIQUES; CARDIOMYOPATHY, HYPERTROPHIC; CARRIER PROTEINS; FEMALE; HUMANS; ISOLATED NONCOMPACTION OF THE VENTRICULAR MYOCARDIUM; MAGNETIC RESONANCE IMAGING; MIDDLE AGED; MUTATION; YOUNG ADULT;

EID: 84885587721     PISSN: 01675273     EISSN: 18741754     Source Type: Journal    
DOI: 10.1016/j.ijcard.2013.03.168     Document Type: Article

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