Exclusion of Identified LGMD1 Loci from Four Dominant Limb-Girdle Muscular Dystrophy Families

By  

Human Heredity, Vol. 48, Iss. 4, 1998-07 ,pp. : 179-184

Karger

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Myotilin, a novel sarcomeric protein with two Ig-like domains, is encoded by a candidate gene for limb-girdle muscular dystrophy

By Salmikangas Paula   Mykkänen Olli-Matti   Grönholm Mikaela   Heiska Leena   Kere Juha   Carpén Olli   Fürst D.O.   Keller T.C.   Blanchard A.   Labeit S.   Fowler V.M.   Gautel M.   Maruyama K.   Young P.   Brown R.H.   Ozawa E.   Olson T.M.   Towbin J.A.   Laing N.G.   Pelin K.   Haravuori H.   Bartoloni L.   Feit H.   Williams A.F.   Kahana E.   Flood G.   Yajima H.   Puius Y.A.   Jeng C.J.   Ohtsuka H.   Mimura N.   Pavalko F.M.   Crawford A.W.   Pomiès P.   Xia H.   Knight P.J.   Närvänen O.   Guyris J.E.   Raghuraman M.   Laitinen T.  

Human Molecular Genetics, Vol. 8, Iss. 7, 1999-07 ,pp. : 1329-1336

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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Mutations in the fukutin-related protein gene ( FKRP ) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C

By Burgunder J-M.  

Human Molecular Genetics, Vol. 10, Iss. 25, 2001-12 ,pp. : 2851-2859

Oxford University Press

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