N. G. Kennaway

Loss of fumarylacetoacetate hydrolase is responsible for the neonatal hepatic dysfunction phenotype of lethal albino mice.

Markus Grompe, M al-Dhalimy, Milton J. Finegold et al. · Genes & Development · 1993 · 352 citations · Full text

Pharmacy, Genetics, Molecular Genetics +11

31P NMR study of improvement in oxidative phosphorylation by vitamins K3 and C in a patient with a defect in electron transport at complex III in skeletal muscle.

Scott M. Eleff, N. G. Kennaway, Neil R.M. Buist et al. · Proceedings of the National Academy of Sciences · 1984 · 274 citations · Full text

Life Sciences, Biochemistry, Physiology +17

MELAS syndrome with mitochondrial tRNA ^Leu[UUR] mutation

Andrew M. Penn, J. W.K. Lee, Philippe Thuillier et al. · Neurology · 1992 · 124 citations

Life Sciences, Neurology, Neuroscience +17

Mitochondrial myopathy with succinate dehydrogenase and aconitase deficiency. Abnormalities of several iron-sulfur proteins.

Robin E. Hall, K. G. Henriksson, S. F. Lewis et al. · Journal of Clinical Investigation · 1993 · 90 citations · Full text

Life Sciences, Biochemistry, Physiology +17

Deficiency in ubiquinone cytochrome c reductase in a patient with mitochondrial myopathy and lactic acidosis.

Victor Darley‐Usmar, N. G. Kennaway, Neil R.M. Buist et al. · Proceedings of the National Academy of Sciences · 1983 · 72 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +17