3. severe phenylalanine hydroxylase deficiency
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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We found 12 resources matching on 'SEVERE PHENYLALANINE HYDROXYLASE DEFICIENCY'

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