Genotype-phenotype correlations in phenylketonuria-Reference-Cited by-同舟云学术

Genotype-phenotype correlations in phenylketonuria

Published:1993-07 Issue:1 Volume:217 Page:15-21
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Trefz Friedrich K.,Burgard Peter,König Thomas,Goebel-Schreiner Barbara,Lichter-Konecki Uta,Konecki David,Schmidt Edzard,Schmidt Hildgund,Bickel Horst

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference11 articles.

1. Phenylketonuria: biochemical mechanisms;Kaufmann;Adv Neurochem,1976

2. Differential diagnosis and significance of various hyperphenylalaninemias;Trefz,1985

3. Molecular basis of phenotypic heterogeneity in PKU;Okano;New Engl J Med,1991

4. Phenylalaninemia: differential diagnosis;Blaskovics;Arch Dis Child,1974

5. Hyperphenylalaninemia: diagnosis and classification of the various types of phenylalanine hydroxylase deficiency in childhood;Güttler;Acta Paediatr Scand,1980

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