A 4-base pair deletion in the mitochondrial cytochrome b gene associated with Parkinsonism/MELAS overlap syndrome.

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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