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Title: Biochemical hallmarks of tyrosine hydroxylase deficiency
Author(s): Brautigam, C.; Wevers, R.A. ; Jansen, R.J.; Smeitink, J.A.M. ; Rijk-van Andel, J.F. de; Gabreëls, F.J.M.; Hofmann, G.F.
Publication year: 1998
Source: Clinical Chemistry, vol. 44, iss. 9, (1998), pp. 1897-1904
Number of Pages: 8 p.
ISSN: 0009-9147
Publication type: Article / Letter to editor

Please use this identifier to cite or link to this item : https://hdl.handle.net/2066/188054   https://hdl.handle.net/2066/188054

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Subject: Inborn errors of metabolism
Inherited neurotransmitten diseases
Erfelijke stofwisselingsziekten
Erfelijke ziekten in de neurotransmissie
Organization: Neurology
Paediatrics
Journal title:
Clinical Chemistry
Volume: vol. 44
Issue: iss. 9
Page start: p. 1897
Page end: p. 1904

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