β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12-Reference-Cited by-同舟云学术

β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12

Published:1995-11 Issue:3 Volume:11 Page:257-265
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Lim Leland E.,Duclos Franck,Broux Odile,Bourg Nathalie,Sunada Yoshihide,Allamand Valérie,Meyer Jon,Richard Isabelle,Moomaw Carolyn,Slaughter Clive,Tomé Fernando M.S.,Fardeau Michel,Jackson Charles E.,Beckmann Jacques S.,Campbell Kevin P.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1195-257.pdf

Reference59 articles.

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2. Ervasti, J.M., Ohlendieck, K., Kahl, S.D., Gaver, M.G. & Campbell, K.P. Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle. Nature 345, 315–31. (1990).

3. Yoshida, M. & Ozawa, E. Glycoprotein complex anchoring dystrophin to sarcolemma. J. Biochem. 108, 748–752 (1990).

4. Ervasti, J.M. & Campbell, K.P. Membrane organization of the dystrophin-glycoprotein complex. Cell 66, 1121–1131 (1991).

5. Hoffman, E.P., Brown, R.H. Jr. & Kunkel, L.M. Dystrophin: the protein product of the Duchenne muscular dystrophy locus. Cell 51, 919–928 (1987).

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