Succinate in dystrophic white matter: A proton magnetic resonance spectroscopy finding characteristic for complex II deficiency-Reference-Cited by-同舟云学术

Succinate in dystrophic white matter: A proton magnetic resonance spectroscopy finding characteristic for complex II deficiency

Published:2002-06-21 Issue:1 Volume:52 Page:38-46
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Brockmann Knut,Bjornstad Alf,Dechent Peter,Korenke Christoph G.,Smeitink Jan,Trijbels J. M. Frans,Athanassopoulos Sabine,Villagran Rafael,Skjeldal Ola H.,Wilichowski Ekkehard,Frahm Jens,Hanefeld Folker

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference36 articles.

1. The genetics and pathology of oxidative phosphorylation

2. Neuropathology and pathogenesis of mitochondrial diseases

3. Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

4. A SURF1 gene mutation presenting as isolated leukodystrophy

5. Deficiency of complex II of the mitochondrial respiratory chain in late-onset optic atrophy and ataxia

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