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A phenylalanine hydroxylase amino acid polymorphism with implications for molecular diagnostics.
Gjetting, T; Romstad, A; Haavik, J; Knappskog, P M; Acosta, A X; Silva, W A; Zago, M A; Guldberg, P; Güttler, F.
Affiliation
  • Gjetting T; The John F. Kennedy Institute, Glostrup, Denmark.
Mol Genet Metab ; 73(3): 280-4, 2001 Jul.
Article in En | MEDLINE | ID: mdl-11461196
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Collection: 01-internacional Database: MEDLINE Main subject: Phenylalanine Hydroxylase / Polymorphism, Genetic / Amino Acid Metabolism, Inborn Errors Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: Mol Genet Metab Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Year: 2001 Document type: Article Affiliation country: Denmark Country of publication: United States
Search on Google
Add to My VHL
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Phenylalanine Hydroxylase / Polymorphism, Genetic / Amino Acid Metabolism, Inborn Errors Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: Mol Genet Metab Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Year: 2001 Document type: Article Affiliation country: Denmark Country of publication: United States