Deletion of mitochondrial DNA in patient with chronic tubulointerstitial nephritis
- 30 April 1995
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 126 (4), 597-601
- https://doi.org/10.1016/s0022-3476(95)70359-4
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Biochemical and molecular investigations in respiratory chain deficienciesClinica Chimica Acta; International Journal of Clinical Chemistry, 1994
- Mitochondrial DNA deletion: A cause of chronic tubulointerstitial nephropathyKidney International, 1994
- Deletion of the mitochondrial DNA in a case of de Toni-Debré-Fanconi syndrome and Pearson syndromePediatric Nephrology, 1994
- Clinical aspects of mitochondrial disordersJournal of Inherited Metabolic Disease, 1992
- de Toni-Fanconi-Debré syndrome with leigh syndrome revealing severe muscle cytochrome c oxidase deficiencyThe Journal of Pediatrics, 1988
- Sequence and organization of the human mitochondrial genomeNature, 1981