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Journal of Inherited Metabolic Disease

, Volume 14, Issue 5, pp 819–824 | Cite as

Molecular study of duchenne and Becker muscular dystrophies in Japanese

  • H. Tsukamoto
  • K. Inui
  • H. Fukushima
  • T. Nishigaki
  • M. Taniike
  • J. Tanaka
  • S. Okada
JSSIEM Meeting

Keywords

Creatine Kinase Muscular Dystrophy Southern Blot Analysis Duchenne Muscular Dystrophy cDNA Probe 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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References

  1. Asano, J., Tomatsu, S., Sukegawa, K., Yamaguchi, S., Ikedo, Y., Minami, R., Iida, M., Nishimura, M., Nakagawa, M., Ohshiro, M. and Orii, T. Gene deletions in Japanese patients with Duchenne and Becker muscular dystrophy.Jpn. J. Hum. Genet. 35 (1990) 159–168CrossRefGoogle Scholar
  2. Chamberlain, J. S., Gibbs, R. A., Ranier, J. E. and Caskey, C. T. Multiplex PCR for the diagnosis of Duchenne muscular dystrophy. In Innis, M. A., Gelfand, D. H., Sninsky, J. J. and White, T. J. (eds.)PCR Protocols: A Guide to Methods and Applications, Academic Press, New York, 1990, pp. 272–281Google Scholar
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  7. Sugino, S., Fujishita, S., Kamimura, N., Matsumoto, T., Wapennar, M. C., Deng, H.-X., Shibuya, N., Miike, T. and Niikawa, N. Molecular-genetic study of Duchenne and Becker muscular dystrophies: Deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females.Am. J. Med. Genet. 34 (1989) 555–561PubMedCrossRefGoogle Scholar
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Copyright information

© SSIEM and Kluwer Academic Publishers 1991

Authors and Affiliations

  • H. Tsukamoto
    • 1
  • K. Inui
    • 1
  • H. Fukushima
    • 1
  • T. Nishigaki
    • 1
  • M. Taniike
    • 1
  • J. Tanaka
    • 1
  • S. Okada
    • 1
  1. 1.Department of PediatricsOsaka University Medical SchoolFukushima, OsakaJapan

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