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. 1988 Aug;63(8):883–885. doi: 10.1136/adc.63.8.883

Mitochondrial DNA and genetic disease.

J Poulton 1
PMCID: PMC1778996  PMID: 3046511

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Anderson S., Bankier A. T., Barrell B. G., de Bruijn M. H., Coulson A. R., Drouin J., Eperon I. C., Nierlich D. P., Roe B. A., Sanger F. Sequence and organization of the human mitochondrial genome. Nature. 1981 Apr 9;290(5806):457–465. doi: 10.1038/290457a0. [DOI] [PubMed] [Google Scholar]
  2. Bartlett R. J., Pericak-Vance M. A., Yamaoka L., Gilbert J., Herbstreith M., Hung W. Y., Lee J. E., Mohandas T., Bruns G., Laberge C. A new probe for the diagnosis of myotonic muscular dystrophy. Science. 1987 Mar 27;235(4796):1648–1650. doi: 10.1126/science.3029876. [DOI] [PubMed] [Google Scholar]
  3. Byrne E., Marzuki S., Sattayasai N., Dennett X., Trounce I. Mitochondrial studies in Kearns-Sayre syndrome: normal respiratory chain function with absence of a mitochondrial translation product. Neurology. 1987 Sep;37(9):1530–1534. doi: 10.1212/wnl.37.9.1530. [DOI] [PubMed] [Google Scholar]
  4. Cann R. L., Stoneking M., Wilson A. C. Mitochondrial DNA and human evolution. Nature. 1987 Jan 1;325(6099):31–36. doi: 10.1038/325031a0. [DOI] [PubMed] [Google Scholar]
  5. DiMauro S., Bonilla E., Zeviani M., Nakagawa M., DeVivo D. C. Mitochondrial myopathies. Ann Neurol. 1985 Jun;17(6):521–538. doi: 10.1002/ana.410170602. [DOI] [PubMed] [Google Scholar]
  6. Egger J., Wilson J. Mitochondrial inheritance in a mitochondrially mediated disease. N Engl J Med. 1983 Jul 21;309(3):142–146. doi: 10.1056/NEJM198307213090304. [DOI] [PubMed] [Google Scholar]
  7. Harper P. S. Congenital myotonic dystrophy in Britain. II. Genetic basis. Arch Dis Child. 1975 Jul;50(7):514–521. doi: 10.1136/adc.50.7.514. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Holt I. J., Harding A. E., Morgan-Hughes J. A. Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies. Nature. 1988 Feb 25;331(6158):717–719. doi: 10.1038/331717a0. [DOI] [PubMed] [Google Scholar]
  9. Hosking G. Visually evoked responses. Arch Dis Child. 1984 Jan;59(1):1–3. doi: 10.1136/adc.59.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Kearsey S. E., Craig I. W. Altered ribosomal RNA genes in mitochondria from mammalian cells with chloramphenicol resistance. Nature. 1981 Apr 16;290(5807):607–608. doi: 10.1038/290607a0. [DOI] [PubMed] [Google Scholar]
  11. Nikoskelainen E. New aspects of the genetic, etiologic, and clinical puzzle of Leber's disease. Neurology. 1984 Nov;34(11):1482–1484. doi: 10.1212/wnl.34.11.1482. [DOI] [PubMed] [Google Scholar]
  12. Ohtani Y., Matsuda I., Iwamasa T. A female case of glycogen storage myopathy due to phosphorylase kinase deficiency. J Inherit Metab Dis. 1982;5(2):71–72. doi: 10.1007/BF01799992. [DOI] [PubMed] [Google Scholar]
  13. Pavlakis S. G., Phillips P. C., DiMauro S., De Vivo D. C., Rowland L. P. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome. Ann Neurol. 1984 Oct;16(4):481–488. doi: 10.1002/ana.410160409. [DOI] [PubMed] [Google Scholar]
  14. Petty R. K., Harding A. E., Morgan-Hughes J. A. The clinical features of mitochondrial myopathy. Brain. 1986 Oct;109(Pt 5):915–938. doi: 10.1093/brain/109.5.915. [DOI] [PubMed] [Google Scholar]
  15. Polak B. C., Wesseling H., Schut D., Herxheimer A., Meyler L. Blood dyscrasias attributed to chloramphenicol. A review of 576 published and unpublished cases. Acta Med Scand. 1972 Nov;192(5):409–414. [PubMed] [Google Scholar]
  16. Rodgers J. R., Smith R., 3rd, Huston M. M., Rich R. R. Maternally transmitted antigen. Adv Immunol. 1986;38:313–359. doi: 10.1016/s0065-2776(08)60010-3. [DOI] [PubMed] [Google Scholar]
  17. Rosing H. S., Hopkins L. C., Wallace D. C., Epstein C. M., Weidenheim K. Maternally inherited mitochondrial myopathy and myoclonic epilepsy. Ann Neurol. 1985 Mar;17(3):228–237. doi: 10.1002/ana.410170303. [DOI] [PubMed] [Google Scholar]
  18. Sapienza C., Peterson A. C., Rossant J., Balling R. Degree of methylation of transgenes is dependent on gamete of origin. Nature. 1987 Jul 16;328(6127):251–254. doi: 10.1038/328251a0. [DOI] [PubMed] [Google Scholar]
  19. Shimoji A., Katsuragi S., Miyakawa T., Hira R., Watanabe K., Miyakawa K., Ishitsu T., Miike T. Familial mitochondrial encephalomyopathy with stroke-like episodes and episodic disturbances of consciousness: a study of pedigree including three generations with multisystemic abnormalities. Jpn J Psychiatry Neurol. 1987 Mar;41(1):47–55. doi: 10.1111/j.1440-1819.1987.tb00390.x. [DOI] [PubMed] [Google Scholar]

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