The point mutation of hypoxanthine-guanine phosphoribosyltransferase (HPRTEdinburgh) and detection by allele-specific polymerase chain reaction.

Article Details

Citation

Lightfoot T, Joshi R, Nuki G, Snyder FF

The point mutation of hypoxanthine-guanine phosphoribosyltransferase (HPRTEdinburgh) and detection by allele-specific polymerase chain reaction.

Hum Genet. 1992 Mar;88(6):695-6.

PubMed ID
1551676 [ View in PubMed
]
Abstract

The change in DNA responsible for partial hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency in three brothers has been determined by polymerase chain amplification and sequencing. An A-to-G substitution at base 155 in exon 3 predicts a change in aspartic acid 52 to glycine. Allele-specific polymerase chain amplification verified the presence of the mutation in genomic DNA and provides a means of direct diagnostic assay.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Hypoxanthine-guanine phosphoribosyltransferaseP00492Details