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Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency in Dutch neonates
Spaapen, L. J. M.
Department of Biochemical Genetics; Stichting Klinische Genetica Zuid-Oost; Nederland
Bakker, J. A.
Department of Molecular Genetics; Stichting Klinische Genetica Zuid-Oost Nederland; The Netherlands
Velter, C.
Department of Molecular Genetics; Stichting Klinische Genetica Zuid-Oost Nederland; The Netherlands
Loots, W.
Department of Molecular Genetics; Stichting Klinische Genetica Zuid-Oost Nederland; The Netherlands
Rubio-Gonzalbo, M. E.
; Department of Pediatrics; Academic Hospital Maastricht; The Netherlands
Forget, P. P.
; Department of Pediatrics; Academic Hospital Maastricht; The Netherlands
Dorland, L.
; University Medical Center Utrecht; The Netherlands
De Koning, T. J.
; University Medical Center Utrecht; The Netherlands
Poll-The, B. T.
; University Medical Center Utrecht; The Netherlands
Ploos Van Amstel, H. K.
; University Medical Center Utrecht; The Netherlands
Bekhof, J.
; Department of Pediatrics; Academic Hospital Groningen; The Netherlands
Blau, N.
; Division of Clinical Chemistry and Biochemistry; University Children's Hospital; Zurich Switzerland
Duran, M.
; University Medical Center Utrecht; The Netherlands
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2001-6-1
Published in:
Journal of Inherited Metabolic Disease. - Wiley. - 2001, vol. 24, no. 3, p. 352-358
Genetics(clinical)
Genetics
Language
English
Open access status
closed
Identifiers
DOI
10.1023/a:1010596317296
ISSN
0141-8955
Persistent URL
https://sonar.ch/global/documents/67346
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