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CpG hotspot causes second mutation in codon 408 of the phenylalanine hydroxylase gene.

Authors :
Ramus SJ
Forrest SM
Saleeba JA
Cotton RG
Source :
Human genetics [Hum Genet] 1992 Sep-Oct; Vol. 90 (1-2), pp. 147-8.
Publication Year :
1992

Abstract

A new mutation has been identified in exon 12 of the gene encoding phenylalanine hydroxylase at codon 408. The single base change from guanine to adenine changes the amino acid arginine to glutamine; thus, the mutation is defined as R408Q. This codon is the site of a mutation known to causes phenylketonuria. Both these mutations are located at the same CpG site.

Details

Language :
English
ISSN :
0340-6717
Volume :
90
Issue :
1-2
Database :
MEDLINE
Journal :
Human genetics
Publication Type :
Academic Journal
Accession number :
1358783
Full Text :
https://doi.org/10.1007/BF00210760