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Identification of Fabry disease in two brothers

  • Case Report
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Journal of Inherited Metabolic Disease

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Reference

  • Desnick, R. J. and Sweeley, C. C. Fabry's disease: α-galactosidase A deficiency. In Stanbury, J. B., Wyngaarden, J. B., Fredrickson, D. S., Goldstein, J. L. and Brown, M. S. (eds.)The Metabolic Basis of Inherited Diseases, McGraw-Hill, New York, 1983, pp. 906–944

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Authors and Affiliations

  1. Institute of Biological and Medical Chemistry, Academy of Medical Sciences of the USSR, Pogodina St, 10, 119832, Moscow

    E. Beyer & G. Wiederschain

  2. Institute of Bioorganic Chemistry, Academy of Sciences of the USSR, 117871, Moscow

    E. Djatlovitskaya

  3. I. M. Sechenov 1 Moscow Medical Institute, Moscow

    O. Zairatyants & A. Berestova

  4. The Botkin Hospital, Moscow

    M. Mendelson & E. Brook

Authors
  1. E. Beyer
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  2. E. Djatlovitskaya
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  3. O. Zairatyants
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  4. A. Berestova
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  5. M. Mendelson
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  6. E. Brook
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  7. G. Wiederschain
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Beyer, E., Djatlovitskaya, E., Zairatyants, O. et al. Identification of Fabry disease in two brothers. J Inherit Metab Dis 13, 230–231 (1990). https://doi.org/10.1007/BF01799692

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  • DOI: https://doi.org/10.1007/BF01799692

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