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R C Nordlie W J Arion T L Hanson J R Gilsdorf R N Horne 《The Journal of biological chemistry》1968,243(6):1140-1146
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Patrick M. Hefferan R. Rodney Howell 《Biochimica et Biophysica Acta (BBA)/General Subjects》1977,496(2):431-435
We demonstrate that glucose-6-phosphatase, pyrophosphate-glucose phosphotransferase, carbamyl phosphate-glucose phosphotransferase and inorganic pyrophosphatase activities are deficient in livers of patients with type I glycogen storage disease. This provides strong genetic evidence that these enzymatic activities reside in a single protein or share a common polypeptide chain. 相似文献
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We demonstrate that glucose-6-phosphatase, pyrophosphate-glucose phosphotransferase, carbamyl phosphate-glucose phosphotransferase and inorganic pyrophosphatase activities are deficient in livers of patients with type I glycogen storage disease. This provides strong genetic evidence that these enzymatic activities reside in a single protein or share a common polypeptide chain. 相似文献