Ventricular septal defect and restrictive cardiomyopathy in a paediatric TNNI3 mutation carrier

Cardiology in the Young

Volumn 20, Issue 5, 2010, Pages 574-576

  Yang, Shi Wei ^a,b   Hitz, Marc Phillip ^a   Andelfinger, Gregor ^a  

^a UNIVERSITY OF MONTREAL   (Canada)

^b NANJING MEDICAL UNIVERSITY   (China)

Author keywords

cardiomyopathies; genotype phenotype correlation; Troponin

Indexed keywords

ATENOLOL; TROPONIN T;

ARTICLE; CASE REPORT; CHILD; DYSPNEA; ECHOCARDIOGRAPHY; FEMALE; FOLLOW UP; GENETIC ASSOCIATION; GENETIC COUNSELING; HEART ATRIUM ENLARGEMENT; HEART CATHETERIZATION; HEART MUSCLE BIOPSY; HEART TRANSPLANTATION; HEART VENTRICLE SEPTUM DEFECT; HETEROZYGOTE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; IMAGE ANALYSIS; INFANT; MISSENSE MUTATION; MUTATIONAL ANALYSIS; NEWBORN; NUCLEAR MAGNETIC RESONANCE IMAGING; PRESCHOOL CHILD; RESTRICTIVE CARDIOMYOPATHY; SARCOMERE; SYSTOLIC HEART MURMUR;

EID: 78649917213     PISSN: 10479511     EISSN: 14671107     Source Type: Journal    
DOI: 10.1017/S1047951110000715     Document Type: Article

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