Fatal infantile liver failure associated with mitochondrial DNA depletion
Open Access
- 31 December 1992
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 121 (6) , 896-901
- https://doi.org/10.1016/s0022-3476(05)80335-x
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Fatal neonatal hepatocellular deficiency with lactic acidosis: a defect of the respiratory chainJournal of Inherited Metabolic Disease, 1991
- Fatal hepatic failure with lactic acidaemia, fanconi syndrome and defective activity of succinate: Cytochromec reductaseJournal of Inherited Metabolic Disease, 1991
- Mitochondrial myopathies: Clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNAAnnals of Neurology, 1989
- Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre SyndromeNew England Journal of Medicine, 1989
- An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop regionNature, 1989
- MITOCHONDRIAL DNA DELETION IN PEARSON'S MARROW/PANCREAS SYNDROMEPublished by Elsevier ,1989
- Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic NeuropathyScience, 1988
- A newborn infant with respiratory distress and persistent stridulous breathingThe Journal of Pediatrics, 1988
- Respiratory chain defects in the mitochondria of cultured skin fibroblasts from three patients with lacticacidemia.Journal of Clinical Investigation, 1986
- Electron cytochemistry of crystalline inclusions in human skeletal muscle mitochondriaJournal of Ultrastructure Research, 1975