Compound Heterozygous Missense Variants in <i>RPL3L</i> Genes Associated with Severe Forms of Dilated Cardiomyopathy: A Case Report and Literature Review
Whole exome sequencing has identified an infant girl with fulminant dilated cardiomyopathy (DCM), leading to severe acute heart failure associated with ribosomal protein large 3-like (<i>RPL3L</i>) gene pathologic variants. Other genetic tests for mitochondrial disorders by sequence anal...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
MDPI AG,
2022-09-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |