Heterogeneity of Coenzyme Q10Deficiency-Reference-Cited by-同舟云学术

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Heterogeneity of Coenzyme Q10Deficiency

Published:2012-08-01 Issue:8 Volume:69 Page:
ISSN:0003-9942
Container-title:Archives of Neurology
language:en
Short-container-title:Arch Neurol

Author:

Emmanuele Valentina,López Luis C.,Berardo Andres,Naini Ali,Tadesse Saba,Wen Bing,D’Agostino Erin,Solomon Martha,DiMauro Salvatore,Quinzii Catarina,Hirano Michio

Publisher

American Medical Association (AMA)

Subject

Neurology (clinical),Arts and Humanities (miscellaneous)

Cited by 186 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. Understanding coenzyme Q;Physiological Reviews;2024-10-01

2. Bi-allelic variants in COQ8B, a gene involved in the biosynthesis of coenzyme Q10, lead to non-syndromic retinitis pigmentosa;The American Journal of Human Genetics;2024-09

3. Demographic characteristics, diagnostic challenges, treatment patterns, and caregiver burden of mitochondrial diseases: a retrospective cross-sectional study;Orphanet Journal of Rare Diseases;2024-08-02

4. Primary Coenzyme Q10 Deficiency-Related Ataxias;Journal of Clinical Medicine;2024-04-19

5. Mutations of GEMIN5 are associated with coenzyme Q10 deficiency: long-term follow-up after treatment;European Journal of Human Genetics;2024-02-05

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