Flemming Güttler

Treatable neurotransmitter deficiency in mild phenylketonuria

N. Blau, A. Romstad, F. Güttler, 2001, Neurology.

Phenylalanine hydroxylase gene mutations in the United States: report from the Maternal PKU Collaborative Study.

R. Matalon, P. Guldberg, R. Koch, 1996, American journal of human genetics.

Molecular basis of phenotypic heterogeneity in phenylketonuria.

F. Güttler, H. Lou, U. Lichter-Konecki, 1991, The New England journal of medicine.

The relationship of genotype to phenotype in phenylalanine hydroxylase deficiency.

P. Guldberg, R. Koch, F. Güttler, 1997, Biochemical and molecular medicine.