Familial dilated cardiomyopathy associated with the typical dystrophin BMD mutation: Report on two additional cases

Acta Myologica

Volumn 3, Issue DEC., 1999, Pages 229-236

  Politano, L ^a   Passamano, L ^a   Petretta, V R ^a   Nigro, V ^a   Papparella, S ^a   Nigro, Ge ^a   Santangelo, L ^a   Esposito, M G ^a   Comi, L I ^a   Nigro, G ^a  

^a Servizio di Cardiomiologia   (Italy)

Author keywords

Dystrophin gene mutations; X linked dilated cardiomyopathy

Indexed keywords

DYSTROPHIN;

ADULT; ARTICLE; BECKER MUSCULAR DYSTROPHY; CASE REPORT; CLINICAL FEATURE; DISEASE ASSOCIATION; GENE DELETION; GENE MUTATION; HEART DILATATION; HISTOPATHOLOGY; HUMAN; IMMUNOHISTOCHEMISTRY; MALE; PATHOGENESIS;

EID: 0033504698     PISSN: 11282460     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (25)