Novel mutations in MYH7 and MYBPC3 of an Indian family causing hypertrophic cardiomyopathy-Reference-Cited by-同舟云学术

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Novel mutations in MYH7 and MYBPC3 of an Indian family causing hypertrophic cardiomyopathy

Published:2001-06 Issue:6 Volume:33 Page:A105
ISSN:0022-2828
Container-title:Journal of Molecular and Cellular Cardiology
language:en
Short-container-title:Journal of Molecular and Cellular Cardiology

Author:

Sakthievel Sadayappan,Waldmüller Stephan,Saadi A.,Joseph P.K.,Rakesh P.G.,Padmakumar R.,Jagan M. Tharakan,Richard Pascale,Schwartz Ketty,Rajamanickam Chellam,Vosberg Hans-Peter

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Molecular Biology

Cited by 4 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. Assessment of the Contribution of a Thermodynamic and Mechanical Destabilization of Myosin-Binding Protein C Domain C2 to the Pathomechanism of Hypertrophic Cardiomyopathy-Causing Double Mutation MYBPC3Δ25bp/D389V;International Journal of Molecular Sciences;2021-11-04

2. Genetic, clinical, molecular, and pathogenic aspects of the South Asian–specific polymorphic MYBPC3Δ25bp variant;Biophysical Reviews;2020-07-12

3. South Asian–Specific MYBPC3 Δ25bp Intronic Deletion and Its Role in Cardiomyopathies and Heart Failure;Circulation: Genomic and Precision Medicine;2020-06

4. Altered C10 domain in cardiac myosin binding protein-C results in hypertrophic cardiomyopathy;Cardiovascular Research;2019-05-03

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