Add to ORKGThe online version of this article, along with updated information and services, is located on th
Contains fulltext : 227365.pdf (Publisher’s version ) (Closed access
<p>Clinical, familial and genetic data of 50 patients with advanced or end stage cardiomyopathy.</p
The online version of this article, along with updated information and services, is located on th
Background—In autoimmune disorders, circulating autoantibodies identify healthy relatives at risk ye...
The online version of this article, along with updated information and services, is located on th
Advances in human genome sequencing have re-invigorated genetics studies of dilated cardiomyopathy (...
Dilated cardiomyopathy (DCM), a leading cause of heart failure and heart transplantation in younger ...
The online version of this article, along with updated information and services, is located on th
AIMS: Familial screening of patients with dilated cardiomyopathy (DCM) allows an early diagnosis o...
Familial screening of patients with dilated cardiomyopathy (DCM) allows an early diagnosis of the di...
The online version of this article, along with updated information and services, is located on th
ysi c d e Background: One-third of cases of dilated cardiomyopathy (DCM) is of familial aetiology. S...
Diagnosing familial dilated cardiomyopathy requires careful family history taking and clinical evalu...
A great deal of progress has recently been made in the discovery and understanding of the genetics o...
Purpose: To characterize early changes in cardiac anatomy and function for lamin A/C gene (LMNA) mut...
Contains fulltext : 227365.pdf (Publisher’s version ) (Closed access
<p>Clinical, familial and genetic data of 50 patients with advanced or end stage cardiomyopathy.</p
The online version of this article, along with updated information and services, is located on th
Background—In autoimmune disorders, circulating autoantibodies identify healthy relatives at risk ye...
The online version of this article, along with updated information and services, is located on th
Advances in human genome sequencing have re-invigorated genetics studies of dilated cardiomyopathy (...
Dilated cardiomyopathy (DCM), a leading cause of heart failure and heart transplantation in younger ...
The online version of this article, along with updated information and services, is located on th
AIMS: Familial screening of patients with dilated cardiomyopathy (DCM) allows an early diagnosis o...
Familial screening of patients with dilated cardiomyopathy (DCM) allows an early diagnosis of the di...
The online version of this article, along with updated information and services, is located on th
ysi c d e Background: One-third of cases of dilated cardiomyopathy (DCM) is of familial aetiology. S...
Diagnosing familial dilated cardiomyopathy requires careful family history taking and clinical evalu...
A great deal of progress has recently been made in the discovery and understanding of the genetics o...
Purpose: To characterize early changes in cardiac anatomy and function for lamin A/C gene (LMNA) mut...
Contains fulltext : 227365.pdf (Publisher’s version ) (Closed access
<p>Clinical, familial and genetic data of 50 patients with advanced or end stage cardiomyopathy.</p
The online version of this article, along with updated information and services, is located on th