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Differently deleted mitochondrial genomes in maternally inherited chronic progressive external ophthalmoplegia

✍ Scribed by M. Tanaka; M. Yoneda; K. Ohno; W. Sato; M. Yamamoto; I. Nonaka; S. Horai; T. Ozawa

Publisher
Springer
Year
1989
Tongue
English
Weight
273 KB
Volume
12
Category
Article
ISSN
0141-8955

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Chronic progressive external ophthalmopl
Chronic progressive external ophthalmoplegia with a novel mitochondrial DNA deletion and a mutation in the tRNALEU(UUR) gene
✍ Thomas GrΓΌnewald; Hildburg Porschke; Hans Goebel; Heinz Reichmann; Peter Seibel πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 576 KB

Large-scale deletions and point mutations of the mitochondrial DNA are generally accepted as being involved in the pathogenesis of diseases associated with mitochondrial encephalomyopathies such as Kearns-Sayre syndrome and chronic progressive external ophthalmoplegia (CPEO). We screened suspected p