Myocardial Fibrosis in the Pathogenesis, Diagnosis, and Treatment of Hypertrophic Cardiomyopathy
Hypertrophic cardiomyopathy (HCM) is a type of hereditary cardiomyopathy caused by gene mutation. Its histological features include cardiomyocyte hypertrophy and disarray as well as myocardial fibrosis. Gene mutation, abnormal signal transduction, and abnormal energy metabolism are considered the ma...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Compuscript
2021-05-01
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| Series: | Cardiovascular Innovations and Applications |
| Subjects: | |
| Online Access: | https://www.ingentaconnect.com/content/cscript/cvia/2021/00000005/00000004/art00005 |