Idiopathic dilated cardiomyopathy: Lack of association with haemochromatosis gene in the cardigene study

Heart

Volumn 86, Issue 6, 2001, Pages 702-703

  Hetet, G ^a   Komajda, M ^b,c,f   Grandchamp, B ^a   Bouchier, C ^b,c   Nicaud, V ^a,c   Tiret, L ^a,c   Roizes, G ^a   Desnos, M ^d   Schwartz, K ^a   Dorent, R ^e  

^a INSERM   (France)

^b SORBONNE UNIVERSITÉ   (France)

^c Muscles et Vaisseaux   (France)

^d HÔPITAL EUROPÉEN GEORGES POMPIDOU   (France)

^e Service de chirurgie cardiaque   (France)

^f PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; CONGESTIVE CARDIOMYOPATHY; CONTROLLED STUDY; GENE AMPLIFICATION; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

EID: 0035189948     PISSN: 13556037     EISSN: None     Source Type: Journal    
DOI: 10.1136/heart.86.6.702     Document Type: Article

References (6)

1. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
2. Effects of HFE C282Y and H63D polymorphisms and polygenic background on iron stores in a large community sample of twins
3. Haemochromatosis gene mutations in idiopathic dilated cardiomyopathy
4. Idiopathic dilated cardiomyopathy: Association with the hereditary haemochromatosis gene
5. Characterization of a unique genetic variant in the betal-adrenoceptor gene and evaluation of its role in idiopathic dilated cardiomyopathy. CARDIGENE Group
6. Association studies between hemochromatosis gene mutations and the risk of cardiovascular diseases