Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of α-dystroglycan

By Longman Cheryl  

Human Molecular Genetics, Vol. 12, Iss. 21, 2003-11 ,pp. : 2853-2861

Oxford University Press

Access to resources Recommend Favorite

Gene therapy of muscular dystrophy

By Chamberlain J.S.  

Human Molecular Genetics, Vol. 11, Iss. 20, 2002-10 ,pp. : 2355-2362

Oxford University Press

Access to resources Recommend Favorite

Caveolin-3 in muscular dystrophy

By Zatz M.  

Human Molecular Genetics, Vol. 7, Iss. 5, 1998-05 ,pp. : 871-877

Oxford University Press

Access to resources Recommend Favorite

Loss of positive allosteric interactions between neuronal nitric oxide synthase and phosphofructokinase contributes to defects in glycolysis and increased fatigability in muscular dystrophy

By Wehling-Henricks Michelle   Oltmann Meredith   Rinaldi Chiara   Myung Kyu H.   Tidball James G.  

Human Molecular Genetics, Vol. 18, Iss. 18, 2009-09 ,pp. : 3439-3451

Oxford University Press

Access to resources Recommend Favorite

The zebrafish as a model for muscular dystrophy and congenital myopathy

By Bassett David I.   Currie Peter D.  

Human Molecular Genetics, Vol. 12, Iss. 2, 2003-10 ,pp. : 265-270

Oxford University Press

Access to resources Recommend Favorite