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Article

Deletion of the mitochondrial DNA in a case of de Toni-Debr�-Fanconi syndrome and Pearson syndrome

1 Apr 1994

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Share to Metabolism and Genetic Disorders
Share to Mitochondrial Function and Pathology
Share to Neonatal Health and Biochemistry

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 8018492
DOI: 10.1007/bf00865468

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 9 closest

Deletion of the mitochondrial DNA in a case of de Toni-Debr�-Fanconi syndrome and Pearson syndromePMID 8018492Read ↗

PEHO syndrome: KIF1A mutation and decreased activity of mitochondrial respiratory chain complexSemantic proximity Read ↗

Mitochondrial DNA deletion in a girl with Fanconi's syndrome.Semantic proximity Read ↗

Mitochondrial DNA deletion with Kearns Sayre syndrome in a child with Addison diseaseSemantic proximity Read ↗

Pearson syndrome and the role of deletion dimers and duplications in the mtDNA.Semantic proximity Read ↗

Deletion of mitochondrial DNA in patient with chronic tubulointerstitial nephritisSemantic proximity Read ↗

Neonatal Fanconi syndrome due to deficiency of complex III of the respiratory chainSemantic proximity Read ↗

Mitochondrial respiratory chain defects in skin fibroblasts from patients with Dravet syndrome.Semantic proximity Read ↗

Large deletion (7.2 kb) of mitochondrial DNA with novel boundaries in a case of progressive external ophthalmoplegia.Semantic proximity Read ↗

Angelman syndrome caused by an identical familial 1,487-kb deletion.Semantic proximity Read ↗

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