Late-onset Leigh syndrome due to NDUFV1 mutation in a 10-year-old boy initially presenting with ataxia
Author:
Publisher
Medknow
Subject
General Neuroscience,Pediatrics, Perinatology, and Child Health
Cited by 11 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. NDUFV1-Related Mitochondrial Complex-1 Disorders: A Retrospective Case Series and Literature Review;Pediatric Neurology;2024-06
2. Tissue-specific atlas of trans-models for gene regulation elucidates complex regulation patterns;BMC Genomics;2024-04-17
3. Current Insights into the Potential of Gene Therapy to Treat Rare Mitochondrial Diseases;Rare Genetic Disorders;2024
4. Leigh Syndrome Spectrum: A Portuguese Population Cohort in an Evolutionary Genetic Era;Genes;2023-07-27
5. NDUFV1 attenuates renal ischemia–reperfusion injury by improving mitochondrial homeostasis;Journal of Cellular and Molecular Medicine;2023-04-07
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