Page
%P
![Loading...](https://link.springer.com/static/c4a417b97a76cc2980e3c25e2271af3129e08bbe/images/pdf-preview/spacer.gif)
-
Chapter
Aminoazidopathien
Hyperphenylalaninämien (HPA) sind durch persistierende Plasmaphenylalaninkonzentrationen >120 Mmol/1 definiert.
-
Article
DNA haplotype analysis at the phenylalanine hydroxylase locus in the Turkish population
Thirty-nine Turkish phenylketonuria (PKU) families were investigated for their DNA haplotypes at the phenylalanine hydroxylase (PAH) locus. There was a threefold higher incidence of consanguinity in the popula...