A Chinese Family With Adult-Onset Leigh-Like Syndrome Caused by the Heteroplasmic m.10191T>C Mutation in the Mitochondrial MTND3 Gene
Author:
Publisher
Frontiers Media SA
Subject
Neurology (clinical),Neurology
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1. Late-Onset Leigh Syndrome With Protracted Gastrointestinal Manifestations: A Rare Case Report;Cureus;2024-05-05
2. Walking Difficulties and Brainstem Dysfunction: a Case Report of Adult Onset Leigh Syndrome;SN Comprehensive Clinical Medicine;2023-06-01
3. Leigh-Like Syndrome With a Novel, Complex Phenotype Due to m.10191T>C in Mt-ND3;Cureus;2022-09-09
4. Early developmental delay in Leigh syndrome spectrum disorders is associated with poor clinical prognosis;Molecular Genetics and Metabolism;2022-04
5. Association Between Epilepsy and Leigh Syndrome With MT-ND3 Mutation, Particularly the m.10191T>C Point Mutation;Frontiers in Neurology;2021-12-10
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