Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts. [electronic resource]
Producer: 19990805Description: 83-92 p. digitalISSN:- 0021-9738
- Acidosis, Lactic -- congenital
- Cell Nucleus -- chemistry
- Cells, Cultured
- DNA -- genetics
- DNA Mutational Analysis
- DNA, Complementary -- genetics
- DNA, Mitochondrial -- genetics
- Electron Transport
- Fatal Outcome
- Fibroblasts -- enzymology
- Genetic Complementation Test
- Genetic Heterogeneity
- Humans
- Hybrid Cells
- Infant
- Infant, Newborn
- Male
- Microscopy, Electron
- NAD(P)H Dehydrogenase (Quinone) -- deficiency
- Organ Specificity
- Transcription, Genetic
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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