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- W2021138492 abstract "Using the assay system which measures the incorporation of U-C14 glucose into new branch points in the glycogen molecule, it has been possible to show the presence of amylo-1,6-glucosidase in human fibroblasts derived from skin biopsies and in cultivated amniotic fluid cells. The marked decrease of this enzyme in cultured fibroblasts from a child with Type III glycogen storage disease indicate the usefulness of this technique not only in establishing the diagnosis among patients, but opens up the possibility of prenatal detection of debrancher enzyme deficiency." @default.
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- W2021138492 date "1970-05-01" @default.
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- W2021138492 title "Amylo-1, 6-glucosidase in human fibroblasts: Studies in Type III glycogen storage disease" @default.
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- W2021138492 doi "https://doi.org/10.1016/0006-291x(70)90576-0" @default.
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