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X-chromosomal Inheritance of Liver Glycogenosis with Phosphorylase Kinase Deficiency

Overview
Journal Am J Hum Genet
Publisher Cell Press
Specialty Genetics
Date 1969 May 1
PMID 5306139
Citations 27
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References
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Wallis P, SIDBURY Jr J, Harris R . Hepatic phosphorylase defect. Studies on peripheral blood. Am J Dis Child. 1966; 111(3):278-82. DOI: 10.1001/archpedi.1966.02090060088008. View

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LYON Jr J, Porter J, Robertson M . Phosphorylase b kinase inheritance in mice. Science. 1967; 155(3769):1550-1. DOI: 10.1126/science.155.3769.1550. View

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Van Hoof F . Amylo-1,6-glucosidase activity and glycogen content of the erythrocytes of normal subjects, patients with glycogen storage disease and heterozygotes. Eur J Biochem. 1967; 2(3):271-4. DOI: 10.1111/j.1432-1033.1967.tb00135.x. View

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Huijing F, OBBINK H, van Creveld S . The activity of the debranching-enzyme system in leucocytes. A genetic study of glycogen storage disease type 3. Acta Genet Stat Med. 1968; 18(2):128-36. DOI: 10.1159/000152128. View

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Chayoth R, Moses S, Steinitz K . Debrancher enzyme activity in blood cells of families with type III glycogen storage disease. A method for diagnosis of heterozygotes. Isr J Med Sci. 1967; 3(3):422-6. View