Related content

Skeletal muscle repair in a mouse model of nemaline myopathy

By Sanoudou Despina   Corbett Mark A.   Han Mei   Ghoddusi Majid   Nguyen Mai-Anh T.   Vlahovich Nicole   Hardeman Edna C.  

Human Molecular Genetics, Vol. 15, Iss. 17, 2006-09 ,pp. : 2603-2612

Oxford University Press

Access to resources Recommend Favorite

Nuclear genetic control of mitochondrial translation in skeletal muscle revealed in patients with mitochondrial myopathy

By Sasarman F.   Karpati G.   Shoubridge E.A.  

Human Molecular Genetics, Vol. 11, Iss. 14, 2002-07 ,pp. : 1669-1681

Oxford University Press

Access to resources Recommend Favorite

A centronuclear myopathy-dynamin 2 mutation impairs skeletal muscle structure and function in mice

By Durieux Anne-Ccile   Vignaud Alban   Prudhon Bernard   Viou Mai Thao   Beuvin Maud   Vassilopoulos Stphane   Fraysse Bodval   Ferry Arnaud   Lain Jeanne   Romero Norma B.   Guicheney Pascale   Bitoun Marc  

Human Molecular Genetics, Vol. 19, Iss. 24, 2010-12 ,pp. : 4820-4836

Oxford University Press

Access to resources Recommend Favorite

An autosomal dominant congenital myopathy with cores and rods is associated with a neomutation in the RYR1 gene encoding the skeletal muscle ryanodine receptor

By Monnier Nicole  

Human Molecular Genetics, Vol. 9, Iss. 18, 2000-11 ,pp. : 2599-2608

Oxford University Press

Access to resources Recommend Favorite

A homozygous splicing mutation causing a depletion of skeletal muscle RYR1 is associated with multi-minicore disease congenital myopathy with ophthalmoplegia

By Monnier Nicole  

Human Molecular Genetics, Vol. 12, Iss. 10, 2003-05 ,pp. : 1171-1178

Oxford University Press

Access to resources Recommend Favorite