Author:
Fabian Elisabeth,Schiller Dietmar,Toplak Hermann,Brunner-Krainz Michaela,Fazekas Franz,Schoefl Rainer,Krejs Guenter J.
Funder
Medical University of Graz
Publisher
Springer Science and Business Media LLC
Reference66 articles.
1. Beck M, Ries M. Fabry disease: clinical manifestations, diagnosis and therapy. Oxford: OCC Europe Ltd; 2001.
2. Brady RO, Gal AE, Bradley RM, Martensson E, Warshaw AL, Laster L. Enzymatic defect in Fabry’s disease: ceramide-trihexosidase deficiency. N Engl J Med. 1967;276(21):1163–7.
3. Kint JA. The enzyme defect in Fabry’s disease. Nature. 1970;227:1173.
4. De Duve C. Exploring cells with a centrifuge. Science. 1975;189(4198):186–94.
5. Desnick RJ, Ioannou YA, Eng CM. Alpha-galactosidase A deficiency: Fabry disease. In: Scriver CR, Beaudet AL, Sly WS, Valle D, Childs B, Kinzler KW, Vogelstein B, editors. The metabolic and molecular bases of inherited disease. New York: McGraw-Hill; 2001. pp. 3733–74.
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4 articles.
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