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Title:
A 4-base pair deletion in the mitochondrial cytochrome b gene associated with Parkinsonism/MELAS overlap syndrome.
Author(s):
Coo, I.F.M. de
;
Renier, W.O.
;
Ruitenbeek, W.
;
Bakker, M.M.
;
Laak, H.J. ter
;
Schagger, H.
;
Oost, B.A. van
;
Smeets, H.J.M.
Publication year:
1999
Source:
Annals of Neurology, vol. 45, iss. 1, (1999), pp. 130-133
Number of Pages:
4 p.
ISSN:
0364-5134
DOI:
https://doi.org/10.1002/1531-8249(199901)45:1<130::AID-ART21>3.3.CO;2-Q
Publication type:
Article / Letter to editor
Please use this identifier to cite or link to this item :
https://hdl.handle.net/2066/157044
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Subject:
Inborn errors of metabolism
Neuromuscular and neurometabolic disorders
Erfelijke stofwisselingsziekten
Neuromusculaire en neurometabole aandoeningen
Organization:
Human Genetics
Neurology
Paediatrics
Radboudumc Extern
Journal title:
Annals of Neurology
Volume:
vol. 45
Issue:
iss. 1
Page start:
p. 130
Page end:
p. 133
This item appears in the following Collection(s)
Faculty of Medical Sciences
[72955]
Academic publications
[185936]
Academic output Radboud University
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