Four novel mutations in the tyrosine hydroxylase gene in patients with infantile parkinsonism.

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Title:	Four novel mutations in the tyrosine hydroxylase gene in patients with infantile parkinsonism.
Author(s):	Swaans, R.J.M.; Rondot, P.; Renier, W.O. ; Heuvel, L.P.W.J. van den ; Steenbergen-Spanjers, G.C.H. ; Wevers, R.A.
Publication year:	2000
Source:	Annals of Human Genetics, vol. 64, (2000), pp. 25-31
ISSN:	0003-4800
DOI:	https://doi.org/10.1046/j.1469-1809.2000.6410025.x
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : https://hdl.handle.net/2066/188679
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Subject:	Epilepsy in mental retardation syndromes Inborn errors of metabolism Inherited neurotransmitten diseases Epilepsie bij mentale retardatie syndromen Erfelijke stofwisselingsziekten Erfelijke ziekten in de neurotransmissie
Organization:	Neurology Paediatrics
Journal title:	Annals of Human Genetics
Volume:	vol. 64
Page start:	p. 25
Page end:	p. 31