Neutrophil metabolic dysfunction in genetically heterogeneous patients with glycogen storage disease type 1b
- 1 September 1986
- journal article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 9 (3) , 297-300
- https://doi.org/10.1007/bf01799669
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
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- A new variant of glycogen storage disease Type I probably due to a defect in the glucose-6-phosphate transport systemBiochemical and Biophysical Research Communications, 1978