Yassin N.A.; Muwakkit S.A.; Ibrahim A.O.; Kayim I.M.; Habbal M.-Z.M.; Chamseddine N.M.; Musallam K.M.; Shamseddine A.I.
(HEIDELBERGTIERGARTENSTRASSE 17, D-69121 HEIDELBERG, GERMANY, 2008)
Gaucher disease (GD) is an autosomal recessive inborn error of metabolism, resulting from a deficiency of the enzyme glucocerebrosidase, causing an accumulation of the glycolipid glucocerebroside within lysosomes of ...