Genetic heterogeneity of left ventricular noncompaction cardiomyopathy

Clinical Cardiology

Volumn 31, Issue 5, 2008, Pages 201-204

  Moric Janiszewska, Ewa ^a   Markiewicz Łoskot, Grazyna ^a  

^a MEDICAL UNIVERSITY OF SILESIA   (Poland)

Author keywords

dystrobrevin gene (DTNA); Cypher ZASP (LIM LDB3); FKBP 12 gene; G4.5 (tafazzin gene); Gene; Lamin A C gene; Ventricular noncompaction cardiomyopathy

Indexed keywords

LAMIN A; LAMIN C; LIM PROTEIN;

AUTOSOMAL DOMINANT INHERITANCE; BARTH SYNDROME; BECKER MUSCULAR DYSTROPHY; CARDIOMYOPATHY; DTNA GENE; EMERY DREIFUSS MUSCULAR DYSTROPHY; FAMILIAL DISEASE; FKBP12 GENE; GENE; GENE MUTATION; GENETIC HETEROGENEITY; GENOTYPE PHENOTYPE CORRELATION; HEART DILATATION; HEART LEFT VENTRICLE HYPERTROPHY; HEART LEFT VENTRICLE NONCOMPACTION CARDIOMYOPATHY; HUMAN; ISOLATED NONCOMPACTION OF THE VENTRICULAR MYOCARDIUM; LAMIN A GENE; LAMIN C GENE; LDB3 GENE; LIM GENE; NOMENCLATURE; REVIEW; SPONGY MYOCARDIUM; TAFAZZIN GENE; X CHROMOSOME LINKED DISORDER;

CARDIOMYOPATHIES; GENETIC HETEROGENEITY; HEART VENTRICLES; HUMANS; MUTATION;

EID: 44449111196     PISSN: 01609289     EISSN: None     Source Type: Journal    
DOI: 10.1002/clc.20202     Document Type: Review

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