A myopathy-related actin mutation increases contractile function

By Lindqvist Johan   Pénisson-Besnier Isabelle   Iwamoto Hiroyuki   Li Meishan   Yagi Naoto   Ochala Julien  

Acta Neuropathologica, Vol. 123, Iss. 5, 2012-05 ,pp. : 739-746

Springer Publishing Company

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Progressive external ophthalmoplegia as initial manifestation of sporadic late-onset nemaline myopathy

By Wengert Oliver   Meisel Andreas   Kress Wolfram   Dekomien Gabriele   Angstwurm Klemens   Heppner Frank   Goebel Hans-Hilmar   Stenzel Werner  

Journal of Neurology, Vol. 258, Iss. 5, 2011-05 ,pp. : 915-917

Springer Publishing Company

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SERCA1 and calsequestrin storage myopathy: a new surplus protein myopathy

By Tomelleri Giuliano   Palmucci Laura   Tonin Paola   Mongini Tiziana   Marini Matteo   L'Erario Roberto   Rizzuto Nicolò   Vattemi Gaetano  

Brain, Vol. 129, Iss. 8, 2006-08 ,pp. : 2085-2092

Oxford University Press

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Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy

By Horvath Rita  

Brain, Vol. 132, Iss. 11, 2009-11 ,pp. : 3165-3174

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A novel mutation in the mitochondrial tRNA Phe gene associated with mitochondrial myopathy

By Moslemi A.-R.   Lindberg C.   Toft J.   Holme E.   Kollberg G.   Oldfors A.  

Neuromuscular Disorders, Vol. 14, Iss. 1, 2004-01 ,pp. : 46-50

Elsevier

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