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Gene diagnosis and carrier detection in hunter syndrome by the iduronate-2-sulphatase cDNA probe

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Journal of Inherited Metabolic Disease

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References

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Authors and Affiliations

  1. Institut für Humangenetik der Medizinischen Universität, Ratzeburger Allee 160, D-2400, Lübeck 1, Germany

    A. Gal & E. Schwinger

  2. Kinderklinik der Universität, Mainz, Germany

    M. Beck

  3. Kinderklinik der Universität, Frankfurt, Germany

    A. C. Sewell

  4. Lysosomal Diseases Research Unit, Department of Chemical Pathology, Adelaide Children's Hospital, Adelaide, Australia

    C. P. Morris & J. J. Hopwood

Authors
  1. A. Gal
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  2. M. Beck
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  3. A. C. Sewell
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  4. C. P. Morris
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  5. E. Schwinger
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  6. J. J. Hopwood
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Gal, A., Beck, M., Sewell, A.C. et al. Gene diagnosis and carrier detection in hunter syndrome by the iduronate-2-sulphatase cDNA probe. J Inherit Metab Dis 15, 342–346 (1992). https://doi.org/10.1007/BF02435972

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  • DOI: https://doi.org/10.1007/BF02435972

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