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- Brockington M., Alsanjari N., Sweeney M. G., Morgan-Hughes J. A., Scaravilli F., Harding A. E. Kearns-Sayre syndrome associated with mitochondrial DNA deletion or duplication: a molecular genetic and pathological study. J Neurol Sci. 1995 Jul;131(1):78–87. doi: 10.1016/0022-510x(95)00091-f. [DOI] [PubMed] [Google Scholar]
- Cooper J. M., Mann V. M., Schapira A. H. Analyses of mitochondrial respiratory chain function and mitochondrial DNA deletion in human skeletal muscle: effect of ageing. J Neurol Sci. 1992 Nov;113(1):91–98. doi: 10.1016/0022-510x(92)90270-u. [DOI] [PubMed] [Google Scholar]
- Johns D. R. Seminars in medicine of the Beth Israel Hospital, Boston. Mitochondrial DNA and disease. N Engl J Med. 1995 Sep 7;333(10):638–644. doi: 10.1056/NEJM199509073331007. [DOI] [PubMed] [Google Scholar]
- Moraes C. T., Sciacco M., Ricci E., Tengan C. H., Hao H., Bonilla E., Schon E. A., DiMauro S. Phenotype-genotype correlations in skeletal muscle of patients with mtDNA deletions. Muscle Nerve Suppl. 1995;3:S150–S153. doi: 10.1002/mus.880181429. [DOI] [PubMed] [Google Scholar]
- Poulton J., Morten K. J., Weber K., Brown G. K., Bindoff L. Are duplications of mitochondrial DNA characteristic of Kearns-Sayre syndrome? Hum Mol Genet. 1994 Jun;3(6):947–951. doi: 10.1093/hmg/3.6.947. [DOI] [PubMed] [Google Scholar]

