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Updated: Aug 5, 2026

A Phenotyping Regimen for Genetically Modified Mice Used to Study Genes Implicated in Human Diseases of Aging
Published on: July 14, 2016
[Mutations causing hereditary hyperphenylalaninemia]
C Zekanowski1, M Nowacka, B Cabalska
1Klinika Pediatrii, Hematologii, Onkologii i Endokrynologii, Akademia Medyczna w Gdańsku.
Abstract:
Mutations in the genes encoding different parts of phenylalanine hydroxylation system cause persistent hyperphenylalaninaemia. The most frequent form of hyperphenylalaninaemia is caused by mutations in the PAH gene. The most common variant result from defect of tetrahydrobiopterin synthase. Mutations in the PAH and PTS genes in the Polish population are presented. Genotype--phenotype correlations are discussed.
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