The glucocerebrosidase locus in Gaucher's disease: molecular analysis of a lysosomal enzyme.

Author:

Mistry P K,Cox T M

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference49 articles.

1. Inborn lysosomal storage diseases;Hers, H.G.;Gastroenterology,1965

2. The metabolic basis of inherited diseases;Scriver, C.R.,1989

3. Gaucher disease: a century of delineation and understanding;Desnick, R.J.,1982

4. Metabolism of glucocerebrosides. II. Evidence of an enzymatic deficiency in Gaucher's disease;Brady, R.O.; Kanfer, J.N.; Shapiro, D.;Biochem Biophys Res Commun,1965

5. A deficiency of glucocerebrosidase in Gaucher's disease;Patrick, A.D.;Biochem,1965

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1. Morbus Gaucher – ein Überblick über eine Sphingolipidose;Therapeutische Umschau;2018-11

2. Activation of p38 Mitogen-Activated Protein Kinase in Gaucher’s Disease;PLOS ONE;2015-08-27

3. Gaucher disease: A diagnostic challenge for internists;European Journal of Internal Medicine;2014-02

4. Disorders of Sphingolipid Metabolism;Inborn Metabolic Diseases;2000

5. Gaucher's Disease and Pregnancy;American Journal of Perinatology;1998-05

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