Unusual features of mitochondrial degeneration in skeletal muscle of patients with nuclear complex I mutation - Letter

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Title:	Unusual features of mitochondrial degeneration in skeletal muscle of patients with nuclear complex I mutation - Letter
Author(s):	Dinopoulos, A.; Smeitink, J.A.M. ; Laak, H.J. ter
Publication year:	2005
Source:	Acta Neuropathologica, vol. 110, iss. 2, (2005), pp. 199-202
ISSN:	0001-6322
DOI:	http://dx.doi.org/10.1007/s00401-005-1036-2
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : https://hdl.handle.net/2066/47984
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Subject:	DCN 1: Perception and Action IGMD 8: Mitochondrial medicine NCMLS 4: Energy and redox metabolism UMCN 3.1: Neuromuscular development and genetic disorders UMCN 5.1: Genetic defects of metabolism UMCN 5.3: Cellular energy metabolism
Organization:	Paediatrics Neurology
Journal title:	Acta Neuropathologica
Volume:	vol. 110
Issue:	iss. 2
Page start:	p. 199
Page end:	p. 202

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