Logo del repository
  1. Home
 
Opzioni

Advances in molecular genetics of dilated cardiomyopathy. The Heart Muscle Disease Study Group.

L. Mestroni
•
C. Rocco
•
M. Vatta
altro
GIACCA, MAURO
1998
  • journal article

Periodico
CARDIOLOGY CLINICS
Abstract
In clinical surveys, familial dilated cardiomyopathy (FDC) has been demonstrated in 20\% to 30\% of patients. In these patients, the cause of the disease lies at the DNA level. Molecular genetic studies represent the tools for the understanding of the etiology of FDC and are currently producing relevant advances: 6 different loci have been mapped so far. The only known disease gene is the dystrophin gene causing X-linked dilated cardiomyopathy, but other cytoskeletal proteins, such as adhalin, could be involved. In familial right ventricular cardiomyopathy (or arrhythmogenic right ventricular dysplasia) characterized by isolated or prevalent right ventricular involvement, three further disease loci have been identified.
Archivio
http://hdl.handle.net/11368/2552650
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0031769265
Diritti
metadata only access
Soggetti
  • Autoimmune Diseases, ...

  • Dilated

  • etiology/genetics, Dy...

  • genetics, Female, Gen...

  • Dominant, Humans, Mal...

  • virology, Pedigree, V...

  • complications

Scopus© citazioni
13
Data di acquisizione
Jun 7, 2022
Vedi dettagli
google-scholar
Get Involved!
  • Source Code
  • Documentation
  • Slack Channel
Make it your own

DSpace-CRIS can be extensively configured to meet your needs. Decide which information need to be collected and available with fine-grained security. Start updating the theme to match your nstitution's web identity.

Need professional help?

The original creators of DSpace-CRIS at 4Science can take your project to the next level, get in touch!

Realizzato con Software DSpace-CRIS - Estensione mantenuta e ottimizzata da 4Science

  • Impostazioni dei cookie
  • Informativa sulla privacy
  • Accordo con l'utente finale
  • Invia il tuo Feedback