CoQ deficiency causes disruption of mitochondrial sulfide oxidation, a new pathomechanism associated with this syndrome-Reference-Cited by-同舟云学术

CoQ deficiency causes disruption of mitochondrial sulfide oxidation, a new pathomechanism associated with this syndrome

Published:2016-11-17 Issue:1 Volume:9 Page:78-95
ISSN:1757-4676
Container-title:EMBO Molecular Medicine
language:en
Short-container-title:EMBO Mol Med

Author:

Luna‐Sánchez Marta¹²,Hidalgo‐Gutiérrez Agustín¹²,Hildebrandt Tatjana M³,Chaves‐Serrano Julio²,Barriocanal‐Casado Eliana¹²,Santos‐Fandila Ángela⁴,Romero Miguel⁵,Sayed Ramy KA²⁶,Duarte Juan⁵,Prokisch Holger⁷,Schuelke Markus⁸^ORCID,Distelmaier Felix⁹,Escames Germaine¹²,Acuña‐Castroviejo Darío¹²,López Luis C¹²^ORCID

Affiliation:

1. Departmento de Fisiología Facultad de Medicina Universidad de Granada Granada Spain

2. Instituto de Biotecnología Centro de Investigación Biomédica Universidad de Granada Granada Spain

3. Institut für Pflanzengenetik Leibniz Universität Hannover Hannover Germany

4. Abbott Nutrition R&D, Abbott Laboratories Granada Spain

5. Departmento de Farmacología Facultad de Farmacia Instituto de Investigación Biosanitaria de Granada Universidad de Granada Granada Spain

6. Department of Anatomy and Embryology Faculty of Veterinary Medicine Sohag University Sohag Egypt

7. Institute of Human Genetics Technische Universität München München Germany

8. Department of Neuropediatrics Charité‐Universitätsmedizin Berlin Berlin Germany

9. Department of General Pediatrics Heinrich‐Heine‐University Düsseldorf Germany

Funder

Ministerio de Economía y Competitividad

Consejería de Economía, Innovación, Ciencia y Empleo, Junta de Andalucía

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Publisher

EMBO

Subject

Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/emmm.201606345

Reference60 articles.

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2. Sulphur amino acid synthesis inSchizosaccharomyces pombe represents a specific variant of sulphur metabolism in fungi

3. Fatal neonatal encephalopathy and lactic acidosis caused by a homozygous loss-of-function variant in COQ9

4. Chronic Exposure to Sulfide Causes Accelerated Degradation of Cytochrome c Oxidase in Ethylmalonic Encephalopathy

5. Mitochondrial diseases caused by toxic compound accumulation: from etiopathology to therapeutic approaches

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