Genetics of dilated cardiomyopathy: A molecular maze?

Heart

Volumn 84, Issue 5, 2000, Pages 463-464

  Komajda, M ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA ACTIN; DESMIN; DIPEPTIDYL CARBOXYPEPTIDASE; DYSTROPHIN; LAMIN A; LAMIN C;

AUTOSOMAL DISORDER; CHROMOSOMAL LOCALIZATION; CHROMOSOME 6Q; CLINICAL FEATURE; DOMINANT INHERITANCE; EARLY DIAGNOSIS; FAMILIAL DISEASE; GENE LOCUS; GENE MUTATION; GENETIC PREDISPOSITION; HEART DILATATION; HUMAN; PHENOTYPE; PRIORITY JOURNAL; RECESSIVE INHERITANCE; REVIEW;

EID: 0033773419     PISSN: 13556037     EISSN: None     Source Type: Journal    
DOI: 10.1136/heart.84.5.463     Document Type: Review

References (13)

1. The frequency of familial dilated cardiomyopathies in a series of patients with idiopathic dilated cardiomyopathy
2. Familial dilated cardiomyopathy: Evidence for genetic and phenotypic heterogeneity
3. Deletion of the dystrophin muscle-promoter region associated with X-linked cardiomyopathy
4. Genetic aspects of heart failure
5. Desmin mutation responsible for idiopathic dilated cardiomyopathy
6. Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22
7. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease
8. Dilated cardiomyopathy and sensorieneural hearing loss. A heritable syndrome that maps to 6q23-24
9. Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement
10. Epidemiology of desmin and cardiac actin gene mutations in a European population of dilated cardiomyopathy
11. Mutations in the gene encoding lamin A/C cause autosomic dominant Emery-Dreyfuss muscular dystrophy
12. LMNA, encoding lamin A/C, is mutated in partial lipodystrophy
13. Lack of association between polymorphism of eight candidate genes and idiopathic dilated cardiomyopathy the Cardigene study