A missense mutation in the mitochondrial ND5 gene associated with a Leigh-MELAS overlap syndrome-Reference-Cited by-同舟云学术

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A missense mutation in the mitochondrial ND5 gene associated with a Leigh-MELAS overlap syndrome

Published:2003-06-10 Issue:11 Volume:60 Page:1857-1861
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Crimi M.,Galbiati S.,Moroni I.,Bordoni A.,Perini M. P.,Lamantea E.,Sciacco M.,Zeviani M.,Biunno I.,Moggio M.,Scarlato G.,Comi G. P.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 62 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. Genetic variants affecting mitochondrial function provide further insights for kidney disease;BMC Genomics;2024-06-10

2. Modeling mitochondrial encephalopathy due to MELAS/Leigh overlap syndrome using induced pluripotent stem cells;Current Progress in iPSC Disease Modeling;2022

3. Leigh Syndrome: A Tale of Two Genomes;Frontiers in Physiology;2021-08-11

4. MELAS/LS Overlap Syndrome Associated With Mitochondrial DNA Mutations: Clinical, Genetic, and Radiological Studies;Frontiers in Neurology;2021-05-07

5. The molecular pathology of pathogenic mitochondrial tRNA variants;FEBS Letters;2021-02-12

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