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23. Limb-Girdle Muscular Dystrophy Type 2A Resulting From c.C479G and c.G1818A Mutations in the Calpain-3 Gene. Ramos E, Pardo S, Mas Rodríguez MF, Vélez J. J Clin Neuromuscul Dis; 2015 Dec; 17(2):59-62. PubMed ID: 26583491 [Abstract] [Full Text] [Related]
24. Limb-girdle muscular dystrophy type 2a with mutation in CAPN3: the first report in Taiwan. Wang CH, Liang WC, Minami N, Nishino I, Jong YJ. Pediatr Neonatol; 2015 Feb; 56(1):62-5. PubMed ID: 23597518 [Abstract] [Full Text] [Related]
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32. Entire CAPN3 gene deletion in a patient with limb-girdle muscular dystrophy type 2A. Jaka O, Azpitarte M, Paisán-Ruiz C, Zulaika M, Casas-Fraile L, Sanz R, Trevisiol N, Levy N, Bartoli M, Krahn M, López de Munain A, Sáenz A. Muscle Nerve; 2014 Sep; 50(3):448-53. PubMed ID: 24715573 [Abstract] [Full Text] [Related]
33. Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic. Stehlíková K, Skálová D, Zídková J, Mrázová L, Vondráček P, Mazanec R, Voháňka S, Haberlová J, Hermanová M, Zámečník J, Souček O, Ošlejšková H, Dvořáčková N, Solařová P, Fajkusová L. BMC Neurol; 2014 Aug 19; 14():154. PubMed ID: 25135358 [Abstract] [Full Text] [Related]
34. Limb-girdle muscular dystrophy type 2A can result from accelerated autoproteolytic inactivation of calpain 3. Garnham CP, Hanna RA, Chou JS, Low KE, Gourlay K, Campbell RL, Beckmann JS, Davies PL. Biochemistry; 2009 Apr 21; 48(15):3457-67. PubMed ID: 19226146 [Abstract] [Full Text] [Related]
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40. [Coincidence of hereditary motor and sensory neuropathy type 1A and limb girdle muscular dystrophy type 2A]. Rudenskaya GE, Bulakh MV, Milovidova TB, Shchagina OA. Zh Nevrol Psikhiatr Im S S Korsakova; 2018 Feb 22; 118(11):72-76. PubMed ID: 30585608 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]