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adenine phosphoribosyltransferase deficiency
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APRT
Human adenine phosphoribosyltransferase deficiency. Demonstration of a single mutant allele common to the Japanese
Human adenine phosphoribosyltransferase. Complete amino acid sequence of the erythrocyte enzyme
Comparative anatomy of the human APRT gene and enzyme: nucleotide sequence divergence and conservation of a nonrandom CpG dinucleotide arrangement
Human adenine phosphoribosyltransferase. Identification of allelic mutations at the nucleotide level as a cause of complete deficiency of the enzyme
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External
Prospective Research Rare Kidney Stones (ProRKS) (ProRKS)