Galactose oxidase (EC 1.1.3.9) is a monomeric enzyme that contains a single copper ion and catalyses the stereospecific oxidation of primary alcohols to their corresponding aldehydes. The protein ...

Glucose-galactose malabsorption (GGM) is a rare inherited metabolic disorder that prevents the body from absorbing two simple sugars: glucose and galactose. Glucose-galactose malabsorption (GGM) is a ...

Galactosemia is a genetic disorder in which the body cannot process galactose, which is a simple sugar that is found in many foods. It is actually part of the sugar called lactose, (lactose contains ...

We describe a 55-year-old man with the cardiac variant of Fabry's disease who had residual α-galactosidase A activity as the result of a missense mutation encoding a substitution of arginine for ...

Glucose-galactose malabsorption (GGM) is a rare metabolic condition. It occurs when a genetic variation makes the body unable to properly absorb the simple sugars glucose and galactose. Sugars are the ...