Calpain-3 mutations in atypical limb-girdle muscular dystrophy patients (2003)
- Authors:
- USP affiliated authors: VAINZOF, MARIZ - IB ; ZATZ, MAYANA - IB
- Unidade: IB
- Assunto: DISTROFIA MUSCULAR
- Language: Inglês
- Imprenta:
- Source:
- Título: Neuromuscular Disorders
- Volume/Número/Paginação/Ano: v. 13, n. 7-8, p. 648, 2003
- Conference titles: International Congress of the World Muscle Society
-
ABNT
PAULA, F de et al. Calpain-3 mutations in atypical limb-girdle muscular dystrophy patients. Neuromuscular Disorders. Oxford: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 25 jan. 2026. , 2003 -
APA
Paula, F. de, Silva, H. A. C., Esteves, C., Jazedje, T., Starling, A., Pavanello, R. de C. M., et al. (2003). Calpain-3 mutations in atypical limb-girdle muscular dystrophy patients. Neuromuscular Disorders. Oxford: Instituto de Biociências, Universidade de São Paulo. -
NLM
Paula F de, Silva HAC, Esteves C, Jazedje T, Starling A, Pavanello R de CM, Vainzof M, Zatz M. Calpain-3 mutations in atypical limb-girdle muscular dystrophy patients. Neuromuscular Disorders. 2003 ; 13( 7-8): 648.[citado 2026 jan. 25 ] -
Vancouver
Paula F de, Silva HAC, Esteves C, Jazedje T, Starling A, Pavanello R de CM, Vainzof M, Zatz M. Calpain-3 mutations in atypical limb-girdle muscular dystrophy patients. Neuromuscular Disorders. 2003 ; 13( 7-8): 648.[citado 2026 jan. 25 ] - The 10 autosomal recessive limb-girdle muscular dystrophies
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- LGMD2G with clinical presentation of congenital muscular dystrophy: a rare phenotype
- Preclinical studies with umbilical cord mesenchymal stromal cells in different animal models for muscular dystrophy
- Why is LGMD2G rare?
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