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Year | Number of Results |
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1998 | 1 |
2003 | 1 |
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Limb-girdle muscular dystrophy type 2A can result from accelerated autoproteolytic inactivation of calpain 3.
Biochemistry. 2009 Apr 21;48(15):3457-67. doi: 10.1021/bi900130u.
Biochemistry. 2009.
PMID: 19226146
Loss of calpain-3 autocatalytic activity in LGMD2A patients with normal protein expression.
Fanin M, Nascimbeni AC, Fulizio L, Trevisan CP, Meznaric-Petrusa M, Angelini C.
Fanin M, et al.
Am J Pathol. 2003 Nov;163(5):1929-36. doi: 10.1016/S0002-9440(10)63551-1.
Am J Pathol. 2003.
PMID: 14578192
Free PMC article.
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Analysis of the UK diagnostic strategy for limb girdle muscular dystrophy 2A.
Groen EJ, Charlton R, Barresi R, Anderson LV, Eagle M, Hudson J, Koref MS, Straub V, Bushby KM.
Groen EJ, et al.
Brain. 2007 Dec;130(Pt 12):3237-49. doi: 10.1093/brain/awm259.
Brain. 2007.
PMID: 18055493
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Functional defects of a muscle-specific calpain, p94, caused by mutations associated with limb-girdle muscular dystrophy type 2A.
Ono Y, Shimada H, Sorimachi H, Richard I, Saido TC, Beckmann JS, Ishiura S, Suzuki K.
Ono Y, et al.
J Biol Chem. 1998 Jul 3;273(27):17073-8. doi: 10.1074/jbc.273.27.17073.
J Biol Chem. 1998.
PMID: 9642272
Free article.
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