Different Phenotypes Caused by the Unique Mutation in the Same Family with Mitochondrial Encephalomyopathy
<p><strong>Background and Objective:</strong> Mitochondrial encephalomyopathies represent a clinically heterogeneous group of disorders resulting from abnormal mitochondrial function. This study investigates the clinical and genetic characteristics of families with mitoch...
| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Discover STM Publishing Ltd
2021-03-01
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| Series: | BioMedica |
| Online Access: | https://biomedicapk.com/10.51441/BioMedica/5-85 |