Biochemical and molecular genetic characteristics of the severe form of tyrosine hydroxylase deficiency.
Publication year
1999Source
Clinical Chemistry, 45, 12, (1999), pp. 2073-2078ISSN
Publication type
Article / Letter to editor

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Organization
Paediatrics - OUD tm 2017
Neurology
Journal title
Clinical Chemistry
Volume
vol. 45
Issue
iss. 12
Page start
p. 2073
Page end
p. 2078
Subject
Inborn errors of metabolism; Inherited neurotransmitten diseases; Erfelijke stofwisselingsziekten; Erfelijke ziekten in de neurotransmissieThis item appears in the following Collection(s)
- Academic publications [227881]
- Faculty of Medical Sciences [86219]
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