Article
Molecular basis for the phenotypical diversity of phenylketonuria and related hyperphenylalaninaemias.
Journal of inherited metabolic disease - 1 Jan 1993
Güttler F, Guldberg P, Henriksen K F, Mikkelsen I, Olsen B, Lou H
Abstract excerpt
No abstract is available from the source.
Topics
- Alleles
- Child, Preschool
- Chromosomes
- Denmark
- Genome
- Humans
- Mutation
- Oligonucleotide Probes
- Phenotype
- Phenylalanine
- Phenylalanine Hydroxylase
- Phenylketonurias
