The complete European guidelines on phenylketonuria: diagnosis and treatment

Author(s):
Van Wegberg, A.M.J.; MacDonald, A.; Ahring, K.; Belanger-Quintana, A.; Blau, N.; Bosch, A.M.; Burlina, A.; Campistol, J.; Feillet, F.; Gizewska, M.; Huijbregts, S.C.; Kearney, S.; Leuzzi, V.; Maillot, F.; Muntau, A.C.; Van Rijn, M.; Trefz, F.; Walter, J.H.; Van Spronsen, F.J.
Published
2017
Publication type
Article / Letter to editor
EuropeanGuidelinesPhenylalanine hydroxylase deficiencyPAH deficiencyPhenylketonuriaPKUHyperphenylalaninemiaPhenylalanineTreatmentManagementRecommendationsTetrahydrobiopterinSapropterin
Date issued
2017-10-12
Language
English
Is part of
Orphanet Journal of Rare Diseases (2017), Vol. 12, p. e162
hdl
1887/59133
doi
10.1186/s13023-017-0685-2