Determination of spontaneous loss of heterozygosity mutations in Aprt heterozygous mice
HPRT-APRT-deficient Mice Are Not a Model for Lesch-Nyhan Syndrome
The primary function of a redundant Sp1 binding site in the mouse aprt gene promoter is to block epigenetic gene inactivation
Mutagenicity and loss of heterozygosity at the APRT locus in human lymphoblastoid cells exposed to 3′-azido-3′-deoxythymidine
Induced activity of adenine phosphoribosyltransferase (APRT) in iron‐deficient barley roots: a possible role for phytosiderophore production
Adenine phosphoribosyltransferase (APRT) deficiency: a new genetic mutation with early recurrent renal stone disease in kidney transplantation
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abbr. for adenine phosphoribosyltransferase.
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