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Autor:
Duygu Ozel Demiralp, Cemil Ozerk Demiralp, Serap Dökmeci, Aysel Yüce, Naşit İğci, Parisa Sharafi
Publikováno v:
Advances in Clinical and Experimental Medicine. 26:1053-1061
BACKGROUND Gaucher disease (GD) is defined as an autosomal recessive disorder resulting from the deficiency of glucocerebrosidase (E.C. 3.2.1.45). Glucocerebrosidase is responsible for the degradation of glucosylceramide into ceramide and glucose. Th