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A novel Loss-of-function Mutation in MYBPC3 Causes familial hypertrophic cardiomyopathy with extreme intrafamilial phenotypic heterogeneity Cover

A novel Loss-of-function Mutation in MYBPC3 Causes familial hypertrophic cardiomyopathy with extreme intrafamilial phenotypic heterogeneity

Balkan Journal of Medical Genetics
Volume 25 (2022): Issue 1 (June 2022)
By: Y Peng,  J Xu,  Y Wang,  J Zhao,  L Zhang,  Z Chen,  Y Jiang,  S Banerjee,  Z Zhang and  M Bai  
Open Access
|Mar 2023
DOI: https://doi.org/10.2478/bjmg-2022-0002 | Journal eISSN: 2199-5761
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Language: English
Page range: 71 - 78
Published on: Mar 1, 2023
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
Keywords:
familial hypertrophic cardiomyopathy,
gene,
novel variant,
heterozygous,
.
Related subjects:
Medicine,
Basic medical science,
Basic medical science, other

© 2023 Y Peng, J Xu, Y Wang, J Zhao, L Zhang, Z Chen, Y Jiang, S Banerjee, Z Zhang, M Bai, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

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