Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes-Reference-Cited by-同舟云学术

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Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes

Published:1990-02 Issue:1 Volume:237 Page:5-10
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Gerbitz K.-D.,Obermaier-Kusser B.,Zierz S.,Pongratz D.,M�ller-H�cker J.,Lestienne P.

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Neurology

Link

http://link.springer.com/content/pdf/10.1007/BF00319660.pdf

Reference26 articles.

1. Anderson S, Bankler AT, Barek BG, Brujin MHL de, Coulson AR, Drouin I, Eperon IC, Nierlich PD, Roe BA, Sanger F, Schreier PH, Smith AIH, Staden R, Young IG (1981) Sequence and organization of the human mitochondrial genome. Nature 290:457?465

2. Carry MR, Ringel SP, Starcerich IM (1986) Mitochondrial morphometrics of histochemically identified human extra ocular muscle fibers. Anat Rec 214:8?16

3. Champagne AM, Dennebouy N, Julien JF, Lehegarat JC, Mounolou JC (1984) Co-linear organization of Xenopus laevis and mouse mitochondrial genomes. Biochem Biophys Res Commun 122:918?924

4. Clayton DA (1984) Transcription of the mammalian mitochondrial genome. Annu Rev Biochem 53:573?594

5. Drouin I (1980) Cloning of human mitochondrial DNA in Escherichia coli. J Mol Biol 140:341

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