Homozygous missense MYBPC3 Pro873His mutation associated with increased risk for heart failure development in hypertrophic cardiomyopathy-Reference-Cited by-同舟云学术

Homozygous missense MYBPC3 Pro873His mutation associated with increased risk for heart failure development in hypertrophic cardiomyopathy

Author:

Kissopoulou Antheia¹²,Trinks Cecilia³,Green Anna³,Karlsson Jan-Erik¹²,Jonasson Jon³,Gunnarsson Cecilia³⁴

Affiliation:

1. Department of Internal Medicine; County Council of Jönköping; Jönköping Sweden

2. Department of Medical and Health Sciences, Faculty of Health Sciences; Linköping University; Linköping Sweden

3. Department of Clinical Genetics, Department of Clinical and Experimental Medicine; Linköping University; Linköping Sweden

4. Centre for Rare Diseases in South East Region of Sweden; Linköping University; Linköping Sweden

Funder

Forskningsrådet i Sydöstra Sverige

Region Östergötland (ALF)

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

Link

Reference21 articles.

1. Hypertrophic cardiomyopathy from A to Z: genetics, pathophysiology, imaging, and management;Baxi;Radiographics: a review publication of the Radiological Society of North America, Inc,2016

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