Reduced α-Gal A enzyme activity in Fabry fibroblast cells and Fabry mice tissues induced by serum from antibody positive patients with Fabry disease
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference16 articles.
1. Alpha-galactosidase A deficiency: Fabry disease;Desnick,2001
2. Recombinant enzyme therapy for Fabry disease: absence of editing of human alpha-galactosidase A mRNA;Blom;Am. J. Hum. Genet.,2003
3. A biochemical and pharmacological comparison of enzyme replacement therapies for the glycolipid storage disorder Fabry disease;Lee;Glycobiology,2003
4. Comparison of the effects of agalsidase alfa and agalsidase beta on cultured human Fabry fibroblasts and Fabry mice;Sakuraba;J. Hum. Genet.,2006
5. International collaborative Fabry disease study group, safety and efficacy of recombinant human alpha-galactosidase A—replacement therapy in Fabry’s disease;Eng;N. Engl. J. Med.,2001
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