Irish Child Health Database - Peer Reviewed Papers
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Mutation, Missense/ genetics
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1. Rapid detection of the R408W and I65T mutations in phenylketonuria by glycosylase mediated polymorphism detection
The aim of this study was to examine application of the novel technique of glycosylase mediated polymorphism detection to the detection of two of the most common mutations of the PAH gene in the Irish population that cause phenylketonuria, R408W and I65T,
Hum Mutat, Vol: 17 Page: 432 May 2001
K. A. O'Donnell; O. Tighe; C. O'Neill; E. Naughten; P. D. Mayne; T. V. McCarthy; P. Vaughan; D. T. Croke



