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The frequency of the CF ΔF508 deletion in CF chromosomes of different ethnic origin

  • Population analysis of the major mutation in cystic fibrosis
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Summary

The identification of the molecular defect in a significant proportion of cystic fibrosis families (in our series up to 60%) allows direct DNA diagnosis.

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Authors and Affiliations

  1. Institut für Humangenetik der Universität, Vesaliusweg 12-14, D-4400, Münster, Germany

    C. Aulehla-Scholz, A. Eigel, B. Dworniczak & J. Horst

  2. Institut für Biochemie der Universität, Gerhard-Domagk-Strasse 1, D-5300, Bonn, Germany

    R. Kaiser, J. Weber & K. Olek

  3. Instituto Nacional de Genetica Medica, Buenos Aires, Argentina

    O. Pivetta

Authors
  1. C. Aulehla-Scholz
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  2. R. Kaiser
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  3. J. Weber
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  4. O. Pivetta
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  5. A. Eigel
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  6. B. Dworniczak
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  7. K. Olek
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  8. J. Horst
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Aulehla-Scholz, C., Kaiser, R., Weber, J. et al. The frequency of the CF ΔF508 deletion in CF chromosomes of different ethnic origin. Hum Genet 85, 392–393 (1990). https://doi.org/10.1007/BF02428269

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  • DOI: https://doi.org/10.1007/BF02428269

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