Mitochondrial disorders
- 30 June 1993
- journal article
- review article
- Published by Elsevier in Current Opinion in Genetics & Development
- Vol. 3 (3) , 457-465
- https://doi.org/10.1016/0959-437x(93)90120-e
Abstract
No abstract availableKeywords
This publication has 53 references indexed in Scilit:
- Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNAThe Lancet, 1992
- Duplications of mitochondrial DNA: Implications for pathogenesisJournal of Inherited Metabolic Disease, 1992
- Structure and function of the mitochondrial genomeJournal of Inherited Metabolic Disease, 1992
- Deletion in Blood Mitochondrial DNA in Kearns-Sayre SyndromePediatric Research, 1992
- DISEASES OF THE MITOCHONDRIAL DNAAnnual Review of Biochemistry, 1992
- Mitochondrial DNA deletions in inherited recurrent myoglobinuriaAnnals of Neurology, 1991
- Mitochondrial myopathies: Clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNAAnnals of Neurology, 1989
- Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre SyndromeNew England Journal of Medicine, 1989
- DUPLICATIONS OF MITOCHONDRIAL DNA IN MITOCHONDRIAL MYOPATHYThe Lancet, 1989
- Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathiesNature, 1988