Kearns-Sayre's syndrome developing in a boy who survived Pearson's syndrome caused by mitochondrial DNA deletion
Author:
Publisher
Springer Science and Business Media LLC
Subject
Physiology (medical),Sensory Systems,Ophthalmology
Link
http://link.springer.com/content/pdf/10.1007/BF00156996.pdf
Reference7 articles.
1. Baerlocher KE, Feldges A, Weissert HJ, Simonsz HJ, Rötig A. Mitochondrial DNA deletion in an 8-year-old boy with Pearson syndrome. J Inher Metab Dis 1992; 15 (in print)
2. Holt IJ, Harding AE, Morgan-Hughes JA. Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies. Nature 1988; 331: 717?19.
3. Moraes CT, DiMauro S, Zeviani M, et al. Mitochondiral DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre Syndrome. New Engl J Med 1989; 320: 1293?99.
4. Palca J. The other human genome. Science 1990; 249: 1104?5.
5. Pearson HA, Lobel JS, Kocoskis SA, et al. A new syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunction. J Pediatr 1979; 95: 976?84.
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