The role of Lamin A/C mutations in Danish patients with idiopathic dilated cardiomyopathy

European Journal of Heart Failure

Volumn 11, Issue 11, 2009, Pages 1031-1035

  Møller, Daniel Vega ^a   Pham, Tam Thanh ^b   Gustafsson, Finn ^a   Hedley, Paula ^b   Ersbøll, Mads Kristian ^a   Bundgaard, Henning ^a   Andersen, Claus B ^a   Torp Pedersen, Christian ^c   Køber, Lars ^a   Christiansen, Michael ^b  

^a Rigshospitalet   (Denmark)

^b STATENS SERUM INSTITUT   (Denmark)

^c UNIVERSITY OF COPENHAGEN   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

LAMIN A; LAMIN C;

ADULT; ARTICLE; CHILD; CONGESTIVE CARDIOMYOPATHY; CONTROLLED STUDY; DENMARK; DISEASE ASSOCIATION; FAMILY COUNSELING; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC SCREENING; HEART ARREST; HEART MUSCLE CONDUCTION DISTURBANCE; HEART VENTRICLE ARRHYTHMIA; HETEROZYGOTE; HUMAN; MAJOR CLINICAL STUDY; MALE; MOLECULAR GENETICS; PATHOGENICITY; PRIORITY JOURNAL; SCHOOL CHILD;

ADULT; CARDIOMYOPATHY, DILATED; CASE-CONTROL STUDIES; CODON, NONSENSE; DENMARK; FEMALE; HUMANS; LAMIN TYPE A; MALE; MIDDLE AGED; MUTATION, MISSENSE; YOUNG ADULT;

EID: 70350695771     PISSN: 13889842     EISSN: 18790844     Source Type: Journal    
DOI: 10.1093/eurjhf/hfp134     Document Type: Article

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