Flemming Güttler

Researcher Next ID · RN-038774

Researcher · Biochemistry, Genetics and Molecular Biology

Copenhagen, Denmark

Accepting doctoral researchersFunding unknown

Research interests

Biochemistry, Genetics and Molecular Biology

Medicine

Metabolism and Genetic Disorders

Folate and B Vitamins Research

Pulmonary Hypertension Research and Treatments

Mitochondrial Function and Pathology

Biochemical and Molecular Research

The Maternal Phenylketonuria International Study: 1984–2002
PEDIATRICS · 2003 · https://doi.org/10.1542/peds.112.s4.1523
A European Multicenter Study of Phenylalanine Hydroxylase Deficiency: Classification of 105 Mutations and a General System for Genotype-Based Prediction of Metabolic Phenotype
The American Journal of Human Genetics · 1998 · https://doi.org/10.1086/301920
Molecular Basis of Phenotypic Heterogeneity in Phenylketonuria
New England Journal of Medicine · 1991 · https://doi.org/10.1056/nejm199105023241802
What do doctors know about statistics?
Statistics in Medicine · 1987 · https://doi.org/10.1002/sim.4780060103
Tight linkage between a splicing mutation and a specific DNA haplotype in phenylketonuria
Nature · 1986 · https://doi.org/10.1038/322799a0
Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuria
Nature · 1983 · https://doi.org/10.1038/306151a0

No projects listed.