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      Fettstoffwechsel 

      Fabry’s Disease—Angiokeratoma Corporis Diffusum Universale

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      Springer Berlin Heidelberg

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          Gene action in the X-chromosome of the mouse (Mus musculus L.).

          MARY LYON (1961)
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            Enzymatic defect in Fabry's disease. Ceramidetrihexosidase deficiency.

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              FABRY'S DISEASE: CLASSIFICATION AS A SPHINGOLIPIDOSIS AND PARTIAL CHARACTERIZATION OF A NOVEL GLYCOLIPID.

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                1976
                : 597-611
                10.1007/978-3-642-66302-4_27
                bc912845-5de7-40fe-a5ff-a5f6a9d23e46
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