Homozygous mutation in the cardiac troponin I gene: Clinical heterogeneity in hypertrophic cardiomyopathy-Reference-Cited by-同舟云学术

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Homozygous mutation in the cardiac troponin I gene: Clinical heterogeneity in hypertrophic cardiomyopathy

Published:2013-09 Issue:2 Volume:168 Page:1530-1531
ISSN:0167-5273
Container-title:International Journal of Cardiology
language:en
Short-container-title:International Journal of Cardiology

Author:

Gray Belinda,Yeates Laura,Medi Caroline,Ingles Jodie,Semsarian Christopher

Funder

National Health and Medical Research Council (NHMRC) Practitioner Fellowship

NHMRC/National Heart Foundation of Australia Early Career Fellowship

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference9 articles.

1. Genetics of hypertrophic cardiomyopathy after 20years: clinical perspectives;Maron;J Am Coll Cardiol,2012

2. Cardiac troponin I mutations in Australian families with hypertrophic cardiomyopathy: clinical, genetic and functional consequences;Doolan;J Mol Cell Cardiol,2005

3. Compound and double mutations in hypertrophic cardiomyopathy patients: implications for genetic testing and counselling;Ingles;J Med Genet,2005

4. Clinical features and outcome of hypertrophic cardiomyopathy associated with triple sarcomere protein gene mutations;Girolami;J Am Coll Cardiol,2010

5. Multiple mutations in genetic cardiovascular disease: a marker of disease severity?;Kelly;Circ Cardiovasc Genet,2009

Cited by 8 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. Clinical Genetics;Clinical Cardiogenetics;2020

2. A case report of recessive restrictive cardiomyopathy caused by a novel mutation in cardiac troponin I (TNNI3);BMC Medical Genetics;2019-04-05

3. Homozygous missense MYBPC3 Pro873His mutation associated with increased risk for heart failure development in hypertrophic cardiomyopathy;ESC Heart Failure;2018-04-16

4. Burden of Recurrent and Ancestral Mutations in Families With Hypertrophic Cardiomyopathy;Circulation: Cardiovascular Genetics;2017-06

5. Prevalence and Clinical Implication of Double Mutations in Hypertrophic Cardiomyopathy;Circulation: Cardiovascular Genetics;2017-04

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