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Mutations in the liver glycogen synthase gene in children with hypoglycemia due to glycogen storage disease type 0

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Figure

Table I. Biochemical Analysis of the Liver Biopsy Specimens
Table II. Oligonucleotide Primer Pairs Used to Amplify the GYS2 Gene
Table III. Exon-Intron Boundary Sequences of the GYS2 Gene
Figure 1. Pedigrees of the patients with GSD-0, the segregation of GSD-0 and chromosome 12p12.2 markers, and the mutations identified inthe GYS2 gene in the families
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