Biochemical characterization of a pedigree with mitochondrially inherited deafness
- 1 November 1992
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 44 (4), 465-472
- https://doi.org/10.1002/ajmg.1320440416
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- Two‐locus mitochondrial and nuclear gene models for mitochondrial disordersGenetic Epidemiology, 1992
- X chromosome-linked and mitochondrial gene control of Leber hereditary optic neuropathy: evidence from segregation analysis for dependence on X chromosome inactivation.Proceedings of the National Academy of Sciences, 1991
- In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria.Molecular and Cellular Biology, 1991
- The measurement of the rotenone-sensitive NADH cytochrome c reductase activity in mitochondria isolated from minute amount of human skeletal muscleBiochemical and Biophysical Research Communications, 1990
- Biogenesis of MitochondriaAnnual Review of Cell Biology, 1988
- Mitochondrial myopathies and respiratory chain proteinsTrends in Biochemical Sciences, 1988
- Use of cyclosporin a in establishing epstein-barr virus-transformed human lymphoblastoid cell linesIn Vitro Cellular & Developmental Biology - Plant, 1984
- Identification of the polypeptides encoded in the ATPase 6 gene and in the unassigned reading frames 1 and 3 of human mtDNA.Proceedings of the National Academy of Sciences, 1983
- Deficiency in ubiquinone cytochrome c reductase in a patient with mitochondrial myopathy and lactic acidosis.Proceedings of the National Academy of Sciences, 1983
- Luft's disease: Further biochemical and ultrastructural studies of skeletal muscle in the second caseJournal of the Neurological Sciences, 1976