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Molecular basis of infantile reversible cytochrome c oxidas..:
Horvath, Rita
;
Kemp, John P
;
Tuppen, Helen AL
...
https://www.repository.cam.ac.uk/handle/1810/290343. , 2009
Link:
https://www.repository.cam.ac.uk/handle/1810/290343
RT Journal T1
Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy
UL https://suche.suub.uni-bremen.de/peid=base-ftunivcam:oai:www.repository.cam.ac.uk:1810_290343&Exemplar=1&LAN=DE A1 Horvath, Rita A1 Kemp, John P A1 Tuppen, Helen AL A1 Hudson, Gavin A1 Oldfors, Anders A1 Marie, Suely KN A1 Moslemi, Ali-Reza A1 Servidei, Serenella A1 Holme, Elisabeth A1 Shanske, Sara A1 Kollberg, Gittan A1 Jayakar, Parul A1 Pyle, Angela A1 Marks, Harold M A1 Holinski-Feder, Elke A1 Scavina, Mena A1 Walter, Maggie C A1 Coku, Jorida A1 Günther-Scholz, Andrea A1 Smith, Paul M A1 McFarland, Robert A1 Chrzanowska-Lightowlers, Zofia MA A1 Lightowlers, Robert N A1 Hirano, Michio A1 Lochmüller, Hanns A1 Taylor, Robert W A1 Chinnery, Patrick F A1 Tulinius, Mar A1 DiMauro, Salvatore PB Oxford University Press (OUP); http://dx.doi.org/10.1093/brain/awp221; Brain YR 2009 K1 Base Sequence K1 Cytochrome-c Oxidase Deficiency K1 Diagnosis K1 Differential K1 Female K1 Genotype K1 Humans K1 Infant K1 Newborn K1 Male K1 Mitochondria K1 Mitochondrial Encephalomyopathies K1 Molecular Biology K1 Molecular Sequence Data K1 Muscle K1 Skeletal K1 Nucleic Acid Conformation K1 Pedigree K1 Phenotype K1 Point Mutation K1 Prognosis JF https://www.repository.cam.ac.uk/handle/1810/290343 LK http://dx.doi.org/https://www.repository.cam.ac.uk/handle/1810/290343 DO https://www.repository.cam.ac.uk/handle/1810/290343 SF ELIB - SuUB Bremen
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