Myotilin, the limb-girdle muscular dystrophy 1A (LGMD1A) protein, cross-links actin filaments and controls sarcomere assembly

By Salmikangas Paula  

Human Molecular Genetics, Vol. 12, Iss. 2, 2003-01 ,pp. : 189-203

Oxford University Press

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Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)

By Muchir Antoine   Bonne Gisèle   van der Kooi Anneke J.   van Mia   Baas Frank   Bolhuis Pieter A.   de Marianne   Schwartz Ketty  

Human Molecular Genetics, Vol. 9, Iss. 9, 2000-05 ,pp. : 1453-1459

Oxford University Press

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Linkage Analysis in Autosomal Recessive Limb-Girdle Muscular Dystrophy (AR LGMD) Maps a Sixth Form to 5q33–34 ( LGMD2F ) and Indicates That There is at Least One More Subtype of AR LGMD

By Passos-Bueno M. R.   Moreira E. S.   Vainzof M.   Marie S. K.   Zatz M.  

Human Molecular Genetics, Vol. 5, Iss. 6, 1996-01 ,pp. : 815-820

Oxford University Press

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Genomic Screening for β-Sarcoglycan Gene Mutations: Missense Mutations May Cause Severe Limb-girdle Muscular Dystrophy Type 2E (LGMD 2E)

By Bönnemann Carsten G.   Passos-Bueno M. Rita   McNally Elizabeth M.   Vainzof Mariz   Moreira Eloísa de Sá   Marie Suely K.   Pavanello Rita C. M.   Noguchi Satoru   Ozawa Eijiro   Zatz Mayana   Kunkel Louis M.  

Human Molecular Genetics, Vol. 5, Iss. 12, 1996-12 ,pp. : 1953-1961

Oxford University Press

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-Sarcoglycan compensates for lack of α-sarcoglycan in a mouse model of limb-girdle muscular dystrophy

By Imamura Michihiro  

Human Molecular Genetics, Vol. 14, Iss. 6, 2005-03 ,pp. : 775-783

Oxford University Press

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