Titlebook: Clinical Cardiogenetics; Hubert F. Baars,Pieter A. F. M. Doevendans,J. Pete Book 20162nd edition Springer International Publishing Switzer

沒有準備

易達到

dagger

STELL

Zusammenfassung und Handlungsempfehlungen,e, hypertension, valvular disease, and congenital heart disease sufficient to explain the observed myocardial abnormality. We describe five main cardiomyopathy subtypes as outlined by the European Society of Cardiology: hypertrophic cardiomyopathy, dilated cardiomyopathy, arrhythmogenic cardiomyopat

先兆

深陷

https://doi.org/10.1007/978-3-658-08575-9as been made in understanding the genetic basis of idiopathic dilated cardiomyopathy (iDCM). Rare variants in >30 genes, some also involved in other cardiomyopathies, muscular dystrophy, or syndromic disease, perturb a diverse set of important myocardial proteins to produce a final DCM phenotype. Re

重力

B-cell