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Heterogeneous tissue expression of enzyme defects in mitochondrial myopathies

✍ Scribed by W. Sperl; W. Ruitenbeek; J. M. F. Trijbels; G. C. Korenke; R. C. A. Sengers

Publisher
Springer
Year
1990
Tongue
English
Weight
292 KB
Volume
13
Category
Article
ISSN
0141-8955

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## Abstract By using a combination of Southern blot hybridization analysis, polymerase–chain reaction amplification, and direct nucleotide sequencing, we studied deletions of mitochondrial DNA (mtDNA) in several nonfamilial patients with progressive external ophthalmoplegia and Kearns‐Sayre syndrom