Molecular diagnosis of mtDNA syndromes in Egyptian pediatric patients: a hospital-based study

Abstract Background MCDs, or mitochondrial disorders, are a major contributor to morbidity and mortality. There are few studies on the prevalence of gene mutations in pediatric MCD patients in Egypt. The objective of the current study was to determine the frequencies of the most prevalent mtDNA muta...

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Bibliographic Details
Main Authors: Dina Mehaney, Donia Abaas, Wajeet Sayed, Mai Sharawy, Laila Selim
Format: Article
Language:English
Published: SpringerOpen 2024-11-01
Series:Egyptian Journal of Medical Human Genetics
Subjects:
Online Access:https://doi.org/10.1186/s43042-024-00609-z
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