Journal article icon

Journal article

Hypertrophic cardiomyopathy: from molecular and genetic mechanisms to clinical management

Abstract:

Molecular genetic research in hypertrophic cardiomyopathy (HCM) has shown that this heart muscle disorder, which was previously considered 'idiopathic', is caused by a wide diversity of mutations that affect the cardiac contractile proteins. With this information, it is now possible to explore molecular genetic diagnosis, recalibration of clinical diagnostic tools and criteria, and genotype-phenotype correlations. However, the biggest potential benefit is that a detailed understanding of the ...

Expand abstract
Publication status:
Published

Actions


Access Document


Authors


Journal:
EUROPEAN HEART JOURNAL SUPPLEMENTS More from this journal
Volume:
3
Issue:
L
Pages:
L43-L50
Publication date:
2001-10-01
DOI:
ISSN:
1520-765X
Language:
English
Keywords:
Pubs id:
pubs:104306
UUID:
uuid:6aea98d2-a41e-4939-bd54-bc9b76526403
Local pid:
pubs:104306
Source identifiers:
104306
Deposit date:
2012-12-19

Terms of use


Views and Downloads






If you are the owner of this record, you can report an update to it here: Report update to this record

TO TOP