severe phenylalanine hydroxylase deficiency - also known as or related to classical phenylketonuria (disorder), phenlyketones+, phenylanaline, nspku - national society for phenylketonuria, urinary phenylketones+, classical phenylketonuria
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You searched for 'severe phenylalanine hydroxylase deficiency'

We found 12 resources matching on 'SEVERE PHENYLALANINE HYDROXYLASE DEFICIENCY'

Support GroupsNSPKU - National Society for Phenylketonuria    View and print PDF of this document
PatientPlusPhenylketonuria     
PatientPlusNewborn Screening     
PatientPlusPrenatal Diagnosis     
GuidelineGuidelines on Phenylketonuria     
Selected UK WebsitesPhenylketonuria     
Information LeafletGlycogen Storage Disorders    View and print PDF of this document
Support GroupsClimb - Children Living with Inherited Metabolic    View and print PDF of this document
Support GroupsPUMPA - Purine Metabolic Patients' Association    View and print PDF of this document
Selected UK WebsitesMetabolic Disease     
Selected UK WebsitesEnzyme Deficiencies     
Selected UK WebsitesGenetic Disorders and Syndromes     
Top 12 resources found for 'SEVERE PHENYLALANINE HYDROXYLASE DEFICIENCY'

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