Characterization of Monoclonal Antibodies to Calpain 3 and Protein Expression in Muscle from Patients with Limb-Girdle Muscular Dystrophy Type 2A-Reference-Cited by-同舟云学术

Characterization of Monoclonal Antibodies to Calpain 3 and Protein Expression in Muscle from Patients with Limb-Girdle Muscular Dystrophy Type 2A

Published:1998-10 Issue:4 Volume:153 Page:1169-1179
ISSN:0002-9440
Container-title:The American Journal of Pathology
language:en
Short-container-title:The American Journal of Pathology

Author:

Anderson Louise V.B.,Davison Keith,Moss Jennifer A.,Richard Isabelle,Fardeau Michel,Tomé Fernando M.S.,Hübner Christoph,Lasa Adriana,Colomer Jaume,Beckmann Jacques S.

Publisher

Elsevier BV

Subject

Pathology and Forensic Medicine

Reference38 articles.

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2. Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy;Roberds;Cell,1994

3. β-Sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12;Lim;Nat Genet,1995

4. Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ-sarcoglycan gene;Nigro;Nat Genet,1996

5. Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A;Richard;Cell,1995

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