Genetic basis of dilated cardiomyopathy
dc.contributor.author
dc.date.accessioned
2024-02-05T12:47:21Z
dc.date.available
2024-02-05T12:47:21Z
dc.date.issued
2016-12-01
dc.identifier.issn
0167-5273
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dc.description.abstract
Dilated cardiomyopathy is a rare cardiac disease characterized by left ventricular dilatation and systolic dysfunction leading to heart failure and sudden cardiac death. Currently, despite several conditions have been reported as aetiologies of the disease, a large number of cases remain classified as idiopathic. Recent studies determine that nearly 60% of cases are inherited, therefore due to a genetic cause. Progressive technological advances in genetic analysis have identified over 60 genes associated with this entity, being TTN the main gene, so far. All these genes encode a wide variety of myocyte proteins, mainly sarcomeric and desmosomal, but physiopathologic pathways are not yet completely unraveled. We review the recent published data about genetics of familial dilated cardiomyopathy
dc.format.extent
12 p.
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application/pdf
dc.language.iso
eng
dc.publisher
Elsevier
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Versió postprint del document publicat a: https://doi.org/10.1016/j.ijcard.2016.09.068
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© International Journal of Cardiology, 2016, vol. 224, p. 461-472
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Articles publicats (D-CM)
dc.rights
Tots els drets reservats
dc.source
Perez-Serra, Alexandra Toro R Sarquella-Brugada G de Gonzalo-Calvo D Cesar S Carro E Llorente-Cortes V Iglesias A Brugada J Brugada, Ramon Campuzano Larrea, Oscar 2016 Genetic basis of dilated cardiomyopathy International Journal of Cardiology 224 461 472
dc.subject
dc.title
Genetic basis of dilated cardiomyopathy
dc.type
info:eu-repo/semantics/article
dc.rights.accessRights
info:eu-repo/semantics/openAccess
dc.type.version
info:eu-repo/semantics/acceptedVersion
dc.identifier.doi
dc.identifier.idgrec
025872
dc.type.peerreviewed
peer-reviewed
dc.identifier.eissn
1874-1754