Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease-Reference-Cited by-同舟云学术

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Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease

Published:2007-04-01 Issue:4 Volume:44 Page:e74-e74
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Blok M J,Spruijt L,de Coo I F M,Schoonderwoerd K,Hendrickx A,Smeets H J

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Cited by 54 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. A systematic review on the biochemical threshold of mitochondrial genetic variants;Genome Research;2024-04-16

2. A case of Leigh syndrome presented with paroxysmal body swing;Heliyon;2024-01

3. Mitochondrial DNA 13513G>A Mutation Causing Leber Hereditary Optic Neuropathy Associated With Adult-Onset Renal Failure;Journal of Neuro-Ophthalmology;2023-07-21

4. Leber Hereditary Optic Neuropathy in a Family of Carriers of MT-ND5 m.13042G>T (A236S) Novel Variant;Journal of Neuro-Ophthalmology;2023-03-10

5. A Case of Infantile Mitochondrial Cardiomyopathy Treated with a Combination of Low-Dose Propranolol and Cibenzoline for Left Ventricular Outflow Tract Stenosis;International Heart Journal;2022-09-30

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