Hypercalcaemia in glycogen storage disease type Ia: A case with R83H and 341delG mutations
Journal
Journal of Inherited Metabolic Disease
Journal Volume
22
Journal Issue
8
Pages
937-938
Date Issued
1999
Author(s)
SDGs
Other Subjects
calcium; glucose 6 phosphatase; article; case report; diet; enzyme deficiency; gene mutation; glycogen storage disease type 1; hematuria; human; hypercalcemia; hypercalciuria; infant; liver biopsy; male; newborn; Taiwan; Diet; Glycogen Storage Disease Type I; Humans; Hypercalcemia; Infant, Newborn; Liver; Male; Mutation; Sequence Deletion
Type
journal article
