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Clinical and Genetic Spectrum of Patients With Mitochondrial Disease in a Pediatric Egyptian Cohort: Novel Variants and Phenotypic Expansion. (2025)

First Author: Hassaan HM

Attributed to: Pleiotropic disorders of mitochondrial translation funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/ajmg.a.63881

PubMed Identifier: 39400921

Publication URI: http://europepmc.org/abstract/MED/39400921

Type: Journal Article/Review

Volume: 197

Parent Publication: American journal of medical genetics. Part A

Issue: 2

ISSN: 1552-4825