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Sarcoglycanopathies: an update.
Vainzof M, Souza LS, Gurgel-Giannetti J, Zatz M. Vainzof M, et al. Neuromuscul Disord. 2021 Oct;31(10):1021-1027. doi: 10.1016/j.nmd.2021.07.014. Epub 2021 Jul 28. Neuromuscul Disord. 2021. PMID: 34404573 Review.
Systemic AAV-Mediated β-Sarcoglycan Delivery Targeting Cardiac and Skeletal Muscle Ameliorates Histological and Functional Deficits in LGMD2E Mice.
Pozsgai ER, Griffin DA, Heller KN, Mendell JR, Rodino-Klapac LR. Pozsgai ER, et al. Mol Ther. 2017 Apr 5;25(4):855-869. doi: 10.1016/j.ymthe.2017.02.013. Epub 2017 Mar 9. Mol Ther. 2017. PMID: 28284983 Free PMC article.
Limb-girdle muscular dystrophy type 2E (LGMD2E), resulting from mutations in beta-sarcoglycan (SGCB), is a progressive dystrophy with deteriorating muscle function, respiratory failure, and cardiomyopathy in 50% or more of LGMD2E patients …
Limb-girdle muscular dystrophy type 2E (LGMD2E), resulting from mutations in beta-sarcoglycan (SGC …
Immunohistochemistry of sarcolemmal membrane-associated proteins in formalin-fixed and paraffin-embedded skeletal muscle tissue: a promising tool for the diagnostic evaluation of common muscular dystrophies.
Suriyonplengsaeng C, Dejthevaporn C, Khongkhatithum C, Sanpapant S, Tubthong N, Pinpradap K, Srinark N, Waisayarat J. Suriyonplengsaeng C, et al. Diagn Pathol. 2017 Feb 20;12(1):19. doi: 10.1186/s13000-017-0610-y. Diagn Pathol. 2017. PMID: 28219397 Free PMC article.