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

Author： 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.  

Publisher： Oxford University Press

ISSN： 1460-2083

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

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

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

Access to resources Recommend Favorite

A slowly progressive form of limb‐girdle muscular dystrophy type 2C associated with founder mutation in the SGCG gene in Puerto Rican Hispanics

By  

Molecular Genetics & Genomic Medicine, Vol. 3, Iss. 2, 2015-03 ,pp. : 92-98

John Wiley & Sons Inc

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

-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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite