Is there a common genetic basis for all familial cardiomyopathies?

European Journal of Heart Failure

Volumn 9, Issue 1, 2007, Pages 4-6

  Perrot, Andreas ^a   Dietz, Rainer ^a   Osterziel, Karl Josef ^a  

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATE SENSITIVE POTASSIUM CHANNEL; ALPHA ACTIN; ALPHA TROPOMYOSIN; CONNECTIN; DELTA SARCOGLYCAN; DESMIN; DYSTROPHIN; LAMIN A; LAMIN C; LIM PROTEIN; METAVINCULIN; MYOSIN BINDING PROTEIN C; MYOSIN HEAVY CHAIN BETA; PHOSPHOLAMBAN; PROTEIN; SARCOGLYCAN; SODIUM CHANNEL; TAFAZZIN; TELETHONIN; TROPOMYOSIN; TROPONIN C; TROPONIN I; TROPONIN T; UNCLASSIFIED DRUG;

CARDIOMYOPATHY; CHROMOSOME 14Q; CONGESTIVE CARDIOMYOPATHY; DISEASE CLASSIFICATION; EDITORIAL; FAMILIAL DISEASE; GENE; GENE EXPRESSION; GENE LOCUS; GENE MUTATION; GENETIC ASSOCIATION; GENETIC VARIABILITY; HEART MUSCLE; HEART MUSCLE CELL; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PUBLICATION; RESTRICTIVE CARDIOMYOPATHY;

CARDIOMYOPATHIES; CARDIOMYOPATHY, DILATED; CARDIOMYOPATHY, HYPERTROPHIC; HUMANS; MUTATION;

EID: 33846258418     PISSN: 13889842     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejheart.2006.04.010     Document Type: Editorial

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