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Uptake and transport of hexoses into polymorphonuclear leukocytes of patients with glycogen storage disease type 1b

✍ Scribed by N. Bashan; R. Potashnik; N. Peleg; A. Moran; S. W. Moses

Publisher: Springer
Year: 1990
Tongue: English
Weight: 255 KB
Volume: 13
Category: Article
ISSN: 0141-8955
DOI: 10.1007/bf01799364

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## Abstract Glycogen storage disease type Ib is an autosomal recessive inherited metabolic disorder resulting from deficiency of the microsomal glucose‐6‐phosphatase enzyme system. Six patients (three of which were treated with granulocyte colony stimulating factor) suffering from this disease were