A theoretical study on binding and stabilization of galactose and novel galactose analogues to the human α-galactosidase A variant causing Fabry disease
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,Biophysics
Reference38 articles.
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3. Fabry disease: α-galactosidase A deficiency. Rosenberg’s Molecular and Genetic Basis of Neurological and Psychiatric Disease;Desnick,2020
4. Functional and pharmacological evaluation of novel GLA variants in Fabry disease identifies six (two de novo) causative mutations and two amenable variants to the chaperone DGJ;Ferri;Clin. Chim. Acta,2018
5. Catalytic mechanism of human α-galactosidase 2;Guce;J. Biol. Chem.,2010
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