Author:
Chrobáková Táňa,Hermanová Markéta,Kroupová Iva,Vondráček Petr,Mařı́ková Tat'ána,Mazanec Radim,Zámečnı́k Josef,Staněk Jan,Havlová Miluše,Fajkusová Lenka
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference17 articles.
1. Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A;Richard;Cell,1995
2. Characterization of monoclonal antibodies to calpain 3 and protein expression in muscle from patients with limb-girdle muscular dystrophy type 2A;Anderson;Am J Pathol,1998
3. Muscle-specific calpain, p94, is degraded by autolysis immediately after translation, resulting in disappearance from muscle;Sorimachi;J Biol Chem,1993
4. Muscle-specific calpain, p94, responsible for limb girdle muscular dystrophy type 2A, associates with connectin through IS2, a p94-specific sequence;Sorimachi;J Biol Chem,1995
5. How calpain is activated by calcium;Khorchid;Nat Struct Biol,2002
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