Clinical Phenotypes of High Risk for Primary Mitochondrial Cytopathies (Part 2)

    О. Є. Абатуров, А. О. Нікуліна
    Studysummary This review discusses the clinical phenotypes of primary mitochondrial cytopathies linked to significant genetic defects in mitochondrial DNA, reporting no new clinical results; the authors emphasize the need for differential diagnosis.
    Automatically generated from the study's abstract, not written by a person, and not a review of the full paper. Not medical advice or a treatment recommendation. Read the original study, and consult a qualified healthcare professional before changing treatment. Full disclaimer
    Read the full study on journal-pkp.uzhnu.edu.ua →
    Discuss this study in the Community →