Open AccessA mitochondrial myopathy characterised by a deficiency in reducible cytochrome b. By JA Morgan-Hughes, P Darveniza, SN Kahn, DN Langdon, RM Sherratt, JM Land and JB Clark (From the Institute of Neurology, Queen Square, London WC1 and the Biochemistry Department, St Bartholomew's Hospital Medical College, London EC1) Brain 1977; 100: 617-640.
Author(s) -
A. Compston
Publication year - 2008
Publication title -
brain
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.142
H-Index - 336
eISSN - 1460-2156
pISSN - 0006-8950
DOI - 10.1093/brain/awn286
Subject(s) - abnormality , weakness , muscle weakness , mitochondrial myopathy , myopathy , mitochondrial disease , physiology , psychology , biology , endocrinology , medicine , neuroscience , anatomy , psychiatry , mitochondrial dna , genetics , gene
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