Radboud Repository
Radboud Repository
→
Collections Radboud University
→
Academic publications
→
View Item
JavaScript is disabled for your browser. Some features of this site may not work without it.
There is no fulltext present in this item.
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
Display more details
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
This item appears in the following Collection(s)
Faculty of Medical Sciences
[71562]
Academic publications
[186162]
Academic output Radboud University
Search Repository
Search Repository
This Collection
Browse
All of Repository
Collections
Departments
Date Issued
Authors
Titles
Document type
This Collection
Departments
Date Issued
Authors
Titles
Document type
Statistics
View Item Statistics