Phenotypic diversity identified by cardiac magnetic resonance in a large hypertrophic cardiomyopathy family with a single MYH7 mutation

Limited data is available on phenotypic variations with the same genotype in hypertrophic cardiomyopathy (HCM). The present study aims to explore the relationship between genotype and phenotype characterized by cardiovascular magnetic resonance (CMR) in a large Chinese family. A proband diagnosed wi...

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Detalles Bibliográficos
Autores principales: Wang, Jie, Wan, Ke, Sun, Jiayu, Li, Weihao, Liu, Hong, Han, Yuchi, Chen, Yucheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5772531/
https://www.ncbi.nlm.nih.gov/pubmed/29343710
http://dx.doi.org/10.1038/s41598-018-19372-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5772531/
https://www.ncbi.nlm.nih.gov/pubmed/29343710
http://dx.doi.org/10.1038/s41598-018-19372-4

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