Autopsy of a patient with restrictive cardiomyopathy with and MYH7 mutation
Restrictive cardiomyopathy (RCM) is a rare type of primary myocardial disease, and its pathological features remain unclear. We report the case of a 78-year-old Japanese woman with RCM and MHY7 mutation who died of heart failure 13 years after the diagnosis. Upon autopsy, focal myocyte amorphous deg...
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| Main Authors: | , , , , , , , , |
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| Format: | Book |
| Published: |
Elsevier,
2021-11-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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