[Classification and heterogeneity of hyperphenylalaninemias linked to a phenylalanine hydroxylase deficiency]

Arch Fr Pediatr. 1987:44 Suppl 1:639-42.

[Article in French]

Authors

F Rey¹, A Munnich, S Lyonnet, J Rey

Affiliation

¹ Département de Pédiatrie, l'Unité de Recherche de Génétique Médicale (INSERM U12), Hôpital des Enfants Malades, Paris.

PMID: 3329492

No abstract available

Publication types

Review

MeSH terms

Amino Acid Metabolism, Inborn Errors / classification*
Child
Genetic Variation*
Humans
Hydroxylation
Mutation
Phenylalanine / blood*
Phenylalanine / metabolism
Phenylalanine / pharmacokinetics
Phenylalanine Hydroxylase / deficiency*
Phenylalanine Hydroxylase / genetics
Phenylketonurias / genetics

Substances

Phenylalanine
Phenylalanine Hydroxylase