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Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Mutations in the phenylalanine hydroxylase gene: genetic determinants for the phenotypic variability of hyperphenylalaninemiaF Güttler, P GuldbergEuropean Journal of Pediatrics|July 1, 1996
The influence of mutations of enzyme activity and phenylalanine tolerance in phenylalanine hydroxylase deficiencyF Güttler, P GuldbergEuropean Journal of Pediatrics|October 24, 2000
Mutation analysis anticipates dietary requirements in phenylketonuriaF Güttler, P GuldbergActa Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Mutations in the phenylalanine hydroxylase gene: methods for their characterizationP Guldberg, F GüttlerGenomics|July 1, 1993
Molecular analysis of phenylketonuria in Denmark: 99% of the mutations detected by denaturing gradient gel electrophoresisP Guldberg, K F Henriksen, F GüttlerClinical Chemistry|December 10, 1999
Single-step mutation scanning of the 6-pyruvoyltetrahydropterin synthase gene in patients with hyperphenylalaninemiaA Romstad, P Guldberg, N Blau, et al.Molecular Genetics and Metabolism|February 13, 2001
In vitro expression of 34 naturally occurring mutant variants of phenylalanine hydroxylase: correlation with metabolic phenotypes and susceptibility toward protein aggregationT Gjetting, M Petersen, P Guldberg, et al.American Journal of Human Genetics|April 28, 2001
Missense mutations in the N-terminal domain of human phenylalanine hydroxylase interfere with binding of regulatory phenylalanineT Gjetting, M Petersen, P Guldberg, et al.Molecular Genetics and Metabolism|May 1, 1998
Mild hyperphenylalaninemia and heterozygosity of the phenylalanine hydroxylase geneR Koch, F Güttler, P Guldberg, et al.Ugeskrift for Laeger|June 16, 1997
[Hemoglobinopathy in the county of Copenhagen]H S Birgens, H Karle, P Guldberg, et al.Pageof 14