Articles by A Oldfors (3)

Clinical manifestation and a new ISCU mutation in iron-sulphur cluster deficiency myopathy

G Kollberg, M Tulinius, A Melberg, N Darin, O Andersen, D Holmgren, A Oldfors and E. Holme

Brain 132 ( 8 ): 2170 - 2179 , 2009

Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy

R Horvath, J. P Kemp, H. A. L Tuppen, G Hudson, A Oldfors, S. K. N Marie, A. R Moslemi, S Servidei, E Holme, S Shanske, G Kollberg, P Jayakar, A Pyle, H. M Marks, E Holinski Feder, M Scavina, M. C Walter, J Coku, A Gunther Scholz, P. M Smith, R McFarland, Z. M. A Chrzanowska Lightowlers, R. N Lightowlers, M Hirano, H Lochmuller, R. W Taylor, P. F Chinnery, M Tulinius and S. DiMauro

Brain 132 ( 11 ): 3165 - 3174 , 2009

Human disease caused by loss of fast IIa myosin heavy chain due to recessive MYH2 mutations

H Tajsharghi, D Hilton Jones, O Raheem, A. M Saukkonen, A Oldfors and B. Udd

Brain 133 ( 5 ): 1451 - 1459 , 2010

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