Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D).

Author:

Carrie A,Piccolo F,Leturcq F,de Toma C,Azibi K,Beldjord C,Vallat J M,Merlini L,Voit T,Sewry C,Urtizberea J A,Romero N,Tome F M,Fardeau M,Sunada Y,Campbell K P,Kaplan J C,Jeanpierre M

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference32 articles.

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2. Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countries;Fardeau, M.; Matsumura, K.; Tome, F.M.S.;C R Acad Sci III,1993

3. Membrane organization of the dystrophin-glycoprotein complex;Ervasti, J.M.; Campbell, K.P.;Cell,1991

4. Heterogeneity of dystrophin-associated proteins;Yamamoto, H.; Hagiwara, Y.; Mizuno, Y.; Yoshida, M.; Ozawa, E.,1993

5. Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia;M, Ben Hamida; M, Fardeau; N, Attia;Muscle Nerve,1983

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