Cardiogenetics, neurogenetics, and pathogenetics of left ventricular hypertrabeculation/noncompaction

Pediatric Cardiology

Volumn 30, Issue 5, 2009, Pages 659-681

  Finsterer, Josef ^a  

^a KRANKENANSTALT RUDOLFSTIFTUNG   (Austria)

Author keywords

Cardiac disease; Genetics; Hypertrophic cardiomyopathy; Mutation; Myocardium; Neuromuscular disorder

Indexed keywords

ALPHA ACTIN; ALPHA DYSTROBREVIN; BINDING PROTEIN; CARDIAC ALPHA ACTIN; CELL NUCLEUS DNA; DYSTROBREVIN; DYSTROPHIN; FIBRILLIN 2; FILAMIN A; LAMININ; LIM DOMAIN BINDING PROTEIN; MITOCHONDRIAL DNA; MT HOLOCYTOCHROME C TYPE SYNTHASE; MYOSIN BINDING PROTEIN C; MYOSIN HEAVY CHAIN BETA; MYOSIN HEAVY CHAIN BETA 7; PEPTIDES AND PROTEINS; PHOSPHORYLASE; PROTEIN KINASE; PROTEIN MADA; PROTEIN TYROSINE PHOSPHATASE 2; PROTEIN TYROSINE PHOSPHATASE SHP 2; SODIUM CHANNEL; SODIUM CHANNEL TYPE 5 ALPHA; SYNTHETASE; TAFFAZIN PROTEIN; TROPONIN T; TYROSINE PHOSPHORYLASE; UNCLASSIFIED DRUG; ZINC FINGER PROTEIN; ZINC FINGER PROTEIN 9;

ADENOSINE MONOPHOSPHATE DEAMINASE DEFICIENCY; ADRENAL DISEASE; ARACHNODACTYLY; BARTH SYNDROME; BEALS HECHT SYNDROME; CHROMOSOME 11P; CHROMOSOME 11Q; CHROMOSOME 17Q; CHROMOSOME 1Q; CHROMOSOME 2Q; CHROMOSOME 4Q; CHROMOSOME 5Q; CHROMOSOME 6P; CHROMOSOME ABERRATION; CHROMOSOME DISORDER; CHROMOSOME TRANSLOCATION 10; CHROMOSOME TRANSLOCATION 11; COBALAMIN C DEFICIENCY; CONFERENCE PAPER; CONGENITAL ADRENAL HYPOPLASIA; CONGENITAL HEART MALFORMATION; DE LANGE SYNDROME; DIAGNOSTIC TEST; DIGEORGE SYNDROME; DISEASE ASSOCIATION; DISEASE CLASSIFICATION; DISORDERS OF MITOCHONDRIAL FUNCTIONS; DYSTROBREVINOPATHY; ENZYME DEFECT; GENE MUTATION; GENETIC ASSOCIATION; GENETIC DISORDER; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENETIC POLYMORPHISM; HEART HEMODYNAMICS; HEART LEFT VENTRICLE HYPERTRABECULATION; HEART MUSCLE ISCHEMIA; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; LEOPARD SYNDROME; LONG QT SYNDROME; MELNICK FRASER SYNDROME; MICROPHTHALMIA; MONOSOMY; MONOSOMY 1Q; MUSCULAR DYSTROPHY; MYOCARDIAL DISEASE; MYOCARDITIS; MYOTONIC DYSTROPHY; MYOTONIC DYSTROPHY 1; MYOTONIC DYSTROPHY 2; NONHUMAN; NOONAN SYNDROME; OHTAHARA SYNDROME; PATHOGENESIS; SICK SINUS SYNDROME; SKIN DEFECT; TRISOMY; TRISOMY 13; TRISOMY 22; TRISOMY 4; TURNER SYNDROME; VITAMIN DEFICIENCY; X CHROMOSOME; ZASPOPATHY;

CARDIOMYOPATHIES; GENETIC DISEASES, INBORN; HEART; HEART DEFECTS, CONGENITAL; HUMANS;

EID: 67349171842     PISSN: 01720643     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00246-008-9359-0     Document Type: Conference Paper

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