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 do periódico: 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: 24 abr. 2024. , 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 2024 abr. 24 ] -
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 2024 abr. 24 ] - Protein defects in neuromuscular diseases
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- LGMD21-secondary muscle protein alterations in patietns with mutations in the fukutin related protein gene
- Possible digenic for limb girdle muscular dystropy
- Multiplex analysis for mutations in the sarcoglycan genes
- Estudo da alfa 2-laminina no diagnóstico pré-natal da distrofia muscular congênita (CMD1A)
- O gene RYR1: triagem de mutações e estudos fisiológicos em pacientes com miopatia de Central Core e hipertermia maligna
- Estudo do gene PTPLA na miopatia congênita centronuclear
- LGMD of variable severity caused by non-allelic mutations
- Calpainopathy: how broad is the spectrum of clinical variability?
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