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

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Publication year
2005Source
Acta Neuropathologica, 110, 2, (2005), pp. 199-202ISSN
Publication type
Article / Letter to editor

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Organization
Paediatrics - OUD tm 2017
Neurology
Journal title
Acta Neuropathologica
Volume
vol. 110
Issue
iss. 2
Page start
p. 199
Page end
p. 202
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 metabolismThis item appears in the following Collection(s)
- Academic publications [227425]
- Electronic publications [107155]
- Faculty of Medical Sciences [86157]
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