Phosphorylase b kinase deficiency in glycogenosis type VIII: differentiation of different phenotypes and heterozygotes by erythrocyte enzyme assay.

G T N Besley

https://doi.org/10.1007/bf01800034

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Journal: Journal of Inherited Metabolic Disease	Publication Date: Feb 5, 1986
Citations: 18

Abstract

AbstractErythrocytes provide a useful sample in which to study phosphorylaseb kinase defects in families affected with GSD VIII.

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