Neonatal hypertrophic cardiomyopathy caused by double mutation in RAS pathway genes-Reference-Cited by-同舟云学术

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Neonatal hypertrophic cardiomyopathy caused by double mutation in RAS pathway genes

Published:2015-04 Issue: Volume:184 Page:272-273
ISSN:0167-5273
Container-title:International Journal of Cardiology
language:en
Short-container-title:International Journal of Cardiology

Author:

Pervunina Tatiana,Vershinina Tatiana,Kiselev Artem,Nikitina Irina,Grekhov Eugeniy,Mitrofanova Lubov,Sjoberg Gunnar,Kostareva Anna

Funder

Russian Science Foundation

Swedish Heart–Lung Foundation

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference16 articles.

1. Simple criteria for differentiation of Fabry disease from amyloid heart disease and other causes of left ventricular hypertrophy;Hoigne;Int. J. Cardiol.,2006

2. Apical hypertrophic cardiomyopathy: an echocardiography challenging case report;Angelis;Int. J. Cardiol.,2015

3. European Society of Cardiology Working Group on M and Pericardial D. Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases;Charron;Eur. Heart J.,2010

4. Syndromes and malformations associated with congenital heart disease in a population-based study;Grech;Int. J. Cardiol.,1999

5. Primary carnitine deficiency cardiomyopathy;Wang;Int. J. Cardiol.,2014

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Mutation location of HCM-causing troponin T mutations defines the degree of myofilament dysfunction in human cardiomyocytes;Journal of Molecular and Cellular Cardiology;2021-01

2. Progressive cardiac conduction disease associated with a DSP gene mutation;International Journal of Cardiology;2016-08

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