Mitochondrial encephalomyopathy with elevated methylmalonic acid is caused by SUCLA2 mutations-Reference-Cited by-同舟云学术

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Mitochondrial encephalomyopathy with elevated methylmalonic acid is caused by SUCLA2 mutations

Published:2007-02-07 Issue:3 Volume:130 Page:853-861
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:Brain

Author:

Ostergaard E.,Hansen F. J.,Sorensen N.,Duno M.,Vissing J.,Larsen P. L.,Faeroe O.,Thorgrimsson S.,Wibrand F.,Christensen E.,Schwartz M.

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Link

http://academic.oup.com/brain/article-pdf/130/3/853/786336/awl383.pdf

Reference28 articles.

1. Metabolomic approaches to mitochondrial disease: correlation of urine organic acids

2. Chapter 5 Assaying mitochondrial respiratory complex activity in mitochondria isolated from human cells and tissues

3. An Evaluation of the Measurement of the Activities of Complexes I-IV in the Respiratory Chain of Human Skeletal Muscle Mitochondria

4. Retrospective, Multicentric Study of 180 Children with Cytochrome c Oxidase Deficiency

5. Urinary excretion of succinylacetone and δ-aminolevulinic acid in patients with hereditary tyrosinemia

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4. Succinyl-CoA Synthetase Dysfunction as a Mechanism of Mitochondrial Encephalomyopathy: More than Just an Oxidative Energy Deficit;International Journal of Molecular Sciences;2023-06-27

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