Cardiac Troponin Mutations and Restrictive Cardiomyopathy

Mutations in sarcomeric proteins have recently been established as heritable causes of Restrictive Cardiomyopathy (RCM). RCM is clinically characterized as a defect in cardiac diastolic function, such as, impaired ventricular relaxation, reduced diastolic volume and increased end-diastolic pressure....

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Detalles Bibliográficos
Autores principales: Parvatiyar, Michelle S., Pinto, Jose Renato, Dweck, David, Potter, James D.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2010
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2896668/
https://www.ncbi.nlm.nih.gov/pubmed/20617149
http://dx.doi.org/10.1155/2010/350706

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2896668/
https://www.ncbi.nlm.nih.gov/pubmed/20617149
http://dx.doi.org/10.1155/2010/350706

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