Title : Molecular basis of disorders of human galactose metabolism: past, present, and future.

Pub. Date : 2000 Sep-Oct

PMID : 11001796






1 Functional Relationships(s)
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1 Molecular cloning and characterization of all three human galactose-metabolic genes have led to the identification of a number of mutations which result in three forms of galactosemia which are caused by kinase (GALK), transferase (GALT), or epimerase (GALE) deficiency. Galactose UDP-galactose-4-epimerase Homo sapiens