A case of Kearns-Sayre syndrome showing a constant proportion of deleted mitochondrial DNA in blood cells during 6 years of follow-up
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference12 articles.
1. Fate and expression of the deleted mitochondrial DNA differ between human heteroplasmic skin fibroblast and Epstein-Barr virus-transformed lymphocyte cultures;Bourgeron;J. Biol. Chem.,1993
2. Kearns-Sayre syndrome associated with mitochondrial DNA deletion or duplication: a molecular genetic and pathological study;Brockington;J. Neurol. Sci.,1995
3. Kearns-Sayre syndrome presenting as renal tubular acidosis;Eviatar;Neurology,1990
4. Deletion in blood mitochondrial DNA in Kearns-Sayre syndrome;Fischel-Ghodsian;Pediatr. Res.,1992
5. Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome;Larsson;Pediatr. Res.,1990
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