Deletion in the cardiac troponin I gene in a family from Northern Sweden with hypertrophic cardiomyopathy

Journal of Molecular and Cellular Cardiology

Volumn 32, Issue 3, 2000, Pages 521-525

  Mörner, Stellan ^a   Richard, Pascale ^c   Kazzam, Elsadig ^b   Hainque, Bernard ^c   Schwartz, Ketty ^c   Waldenström, Anders ^a  

^a UMEÅ UNIVERSITY HOSPITAL   (Sweden)

^b Malar Hospital   (Sweden)

^c PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

Cardiac troponin I; Familial hypertrophic cardiomyopathy; Genetics; Mutation

Indexed keywords

TROPONIN I;

ARTICLE; COMPLEX FORMATION; ECHOCARDIOGRAPHY; FAMILIAL DISEASE; GENE DELETION; GENE MUTATION; GENETIC HETEROGENEITY; HUMAN; HUMAN CELL; HYPERTROPHIC CARDIOMYOPATHY; MULTIGENE FAMILY; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; STOP CODON; SWEDEN;

POMACANTHUS MACULOSUS;

EID: 0033847945     PISSN: 00222828     EISSN: None     Source Type: Journal    
DOI: 10.1006/jmcc.1999.1099     Document Type: Article

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