Maternal inheritance and the evaluation of oxidative phosphorylation diseases
- 9 November 1996
- journal article
- review article
- Published by Elsevier in The Lancet
- Vol. 348 (9037) , 1283-1288
- https://doi.org/10.1016/s0140-6736(96)09138-6
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Renal amino acid transport in adults with oxidative phosphorylation diseasesKidney International, 1995
- Mitochondria1 encephalomyopathy associated with a single nucleotide pair deletion in the mitochondrial tRNA Leu(UUR) geneNeurology, 1995
- An autosomal locus predisposing to deletions of mitochondrial DNANature Genetics, 1995
- Evaluation of procedures for assaying oxidative phosphorylation enzyme activities in mitochondrial myopathy muscle biopsiesBiochimica et Biophysica Acta (BBA) - Bioenergetics, 1990
- An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop regionNature, 1989
- Tandem direct duplications of mitochondrial DNA in mitochondrial myopathy: analysis of nucleotide sequence and tissue distributionNucleic Acids Research, 1988
- Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic NeuropathyScience, 1988
- Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathiesNature, 1988
- A CASE OF SEVERE HYPERMETABOLISM OF NONTHYROID ORIGIN WITH A DEFECT IN THE MAINTENANCE OF MITOCHONDRIAL RESPIRATORY CONTROL: A CORRELATED CLINICAL, BIOCHEMICAL, AND MORPHOLOGICAL STUDYJournal of Clinical Investigation, 1962
- Retinitis Pigmentosa, External Ophthalmoplegia, and Complete Heart BlockA.M.A. Archives of Ophthalmology, 1958