Leigh Syndrome with Nephropathy and CoQ10 Deficiency Due to decaprenyl diphosphate synthase subunit 2 (PDSS2) Mutations-Reference-Cited by-同舟云学术

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Leigh Syndrome with Nephropathy and CoQ10 Deficiency Due to decaprenyl diphosphate synthase subunit 2 (PDSS2) Mutations

Published:2006-12 Issue:6 Volume:79 Page:1125-1129
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

López Luis Carlos,Schuelke Markus,Quinzii Catarina M.,Kanki Tomotake,Rodenburg Richard J.T.,Naini Ali,DiMauro Salvatore,Hirano Michio

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference21 articles.

1. Biosynthesis, bioproduction and novel roles of ubiquinone;Kawamukai;J Biosci Bioeng,2002

2. Metabolism and function of coenzyme Q;Turunen;Biochim Biophys Acta,2004

3. Muscle coenzyme Q deficiency in familial mitochondrial encephalomyopathy;Ogasahara;Proc Natl Acad Sci USA,1989

4. Mitochondrial encephalomyopathy with coenzyme Q10 deficiency;Sobreira;Neurology,1997

5. A case of mitochondrial encephalomyopathy associated with a muscle coenzyme Q10 deficiency;Boitier;J Neurol Sci,1998

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4. Efficacy and Safety of Coenzyme Q10 Supplementation in Neonates, Infants and Children: An Overview;Antioxidants;2024-04-26

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