An autosomal locus predisposing to deletions of mitochondrial DNA
- 1 February 1995
- journal article
- research article
- Published by Springer Nature in Nature Genetics
- Vol. 9 (2) , 146-151
- https://doi.org/10.1038/ng0295-146
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Activation of the human mitochondrial transcriptionfactor A gene by nuclear respiratory factors: a potential regulatory linkbetween nuclear and mitochondrial gene expression in organellebiogenesis.Proceedings of the National Academy of Sciences, 1994
- RTG1 and RTG2: Two yeast genes required for a novel path of communication from mitochondria to the nucleusCell, 1993
- Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNAThe Lancet, 1992
- Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia.Journal of Clinical Investigation, 1992
- DISEASES OF THE MITOCHONDRIAL DNAAnnual Review of Biochemistry, 1992
- Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNANeurology, 1991
- Nuclear gadgets in mitochondrial DNA replication and transcriptionTrends in Biochemical Sciences, 1991
- Marked decrease of mitochondrial DNA with multiple deletions in a patient with familial mitochondrial myopathyBiochemical and Biophysical Research Communications, 1990
- Multiple deletions in mitochondrial DNA at direct repeats of non-D-loop regions in cases of familial mitochondrial myopathyBiochemical and Biophysical Research Communications, 1989
- An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop regionNature, 1989