Biochemical and molecular genetic characteristics of the severe form of tyrosine hydroxylase deficiency.

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Title:	Biochemical and molecular genetic characteristics of the severe form of tyrosine hydroxylase deficiency.
Author(s):	Brautigam, C.; Steenbergen-Spanjers, G.C.H. ; Hoffmann, G.F.; Dionisi-Vici, C.; Heuvel, L.P.W.J. van den ; Smeitink, J.A.M. ; Wevers, R.A.
Publication year:	1999
Source:	Clinical Chemistry, vol. 45, iss. 12, (1999), pp. 2073-2078
ISSN:	0009-9147
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : https://hdl.handle.net/2066/184713
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Subject:	Inborn errors of metabolism Inherited neurotransmitten diseases Erfelijke stofwisselingsziekten Erfelijke ziekten in de neurotransmissie
Organization:	Paediatrics Neurology
Journal title:	Clinical Chemistry
Volume:	vol. 45
Issue:	iss. 12
Page start:	p. 2073
Page end:	p. 2078
Classification:	Central Nervous SystemChemistry, ClinicalEnergy MetabolismFibroblastsGenetics, BiochemicalHereditary DiseasesHomocystinuriaMental DisordersMetabolic DiseasesMetabolic Processes (Non MeSH)Metabolism, Inborn ErrorsMitochondriaMitochondrial MyopathiesMuscle, SkeletalMuscle, SkeletalMutationNeural Tube DefectsNeuromuscular DiseasesPregnancy Complications, CardiovascularVascular Diseases