Comparison of genotype and intellectual phenotype in untreated PKU patients.

Author:

Ramus S J,Forrest S M,Pitt D B,Saleeba J A,Cotton R G

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference33 articles.

1. Hyperphenylalaninemia: diagnosis and classification of the various types of phenylalanine hydroxylase deficiency in childhood;Guttler, F.;Acta Paediatr Scand Suppl,1980

2. Phenylketonuria in Victoria;Pitt, D.; Wilmot, A.E.,1965

3. The natural history of untreated phenylketonuria. MedJ7 Aust;Pitt, D.,1971

4. Phenylketonuria with normal intelligence: report of two cases;Pitt, D.;Aust Ment Res,1971

5. Molecular basis of phenylketonuria and related hyperphenylalanemias: mutations and polymorphisms in the human phenylalanine hydroxylase gene;Eisensmith, R.C.; Woo, S.L.C.;Hum Mutat,1992

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