Novel pathogenic variant in MED12 causing non-syndromic dilated cardiomyopathy
Abstract Background Dilated cardiomyopathy (DCM) is a major cause of sudden cardiac death and heart failure. Up to 50% of all DCM cases have a genetic background, with variants in over 250 genes reported in association with DCM. Whole-exome sequencing (WES) is a powerful tool to identify variants un...
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| Main Authors: | , , , , |
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| Format: | Book |
| Published: |
BMC,
2023-12-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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