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

F Rey1, A Munnich, S Lyonnet

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

Archives Francaises De Pediatrie
|January 1, 1987
PubMed
Abstract

No abstract available in PubMed .

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