A review of biochemical and molecular genetic aspects of tyrosine hydroxylase deficiency including a novel mutation

Authors :: Wevers, R.A.
Rijk-van Andel, J.F. de
Brautigam, C.
Geurtz, B.
Heuvel, L.P.W.J. van den
Steenbergen-Spanjers, G.C.H.
Smeitink, J.A.M.
Hoffmann, G.F.
Gabreëls, F.J.M.
Source :: Journal of Inherited Metabolic Disease, 22, 364-373, Journal of Inherited Metabolic Disease, 22, 4, pp. 364-373
Publication Year :: 1999
Abstract: Item does not contain fulltext 10 p.

Subjects :: Inherited neurotransmitten diseases
Inborn errors of metabolism
Erfelijke stofwisselingsziekten
Erfelijke ziekten in de neurotransmissie

ISSN :: 01418955
Database :: OpenAIRE
Journal :: Journal of Inherited Metabolic Disease, 22, 364-373, Journal of Inherited Metabolic Disease, 22, 4, pp. 364-373
Accession number :: edsair.dedup.wf.001..695a1d126f2d800dd02ce6f3d742ce54

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