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[Catalog of mutations of the phenylalanine hydroxylase gene]

F Rey1, J Rey

  • 1Unité de Recherches sur les Handicaps Génétiques de l'Enfant (INSERM U12), Hôpital des Enfants-Malades, Paris.

Archives Francaises De Pediatrie
|January 1, 1992
PubMed
Abstract

No abstract available in PubMed .

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