Fatal cytochromec oxidase‐deficient myopathy of infancy associated with mtDNA depletion. Differential involvement of skeletal muscle and cultured fibroblasts
- 1 May 1992
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 15 (3) , 323-326
- https://doi.org/10.1007/bf02435967
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases.1991
- Differential diagnosis of fatal and benign cytochrome c oxidase‐deficient myopathies of infancyNeurology, 1991
- Cytochrome c Oxidase DeficiencyPediatric Research, 1990
- An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop regionNature, 1989