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    • Enzyme Replacement Therapy in a Gaucher Family 

      Erdem, N. and Buran, T. and Berber, I. and Aydogdu, I. (National Medical Association, 2018)
      Gaucher disease is a lipid storage disorder due to deficiency of beta glucocerebrosidase. It's an autosomal recessive disease and as a result of this enzyme deficiency, glucocerebroside accumulates in various types of ...