Reviewing large LAMA2 deletions and duplications in congenital muscular dystrophy patients (2014)
- Authors:
- Autor USP: VAINZOF, MARIZ - IB
- Unidade: IB
- DOI: 10.3233/JND-140031
- Subjects: DISTROFIA MUSCULAR (CONGÊNITO); MUTAÇÃO GENÉTICA; DISTROFIA MUSCULAR (DIAGNÓSTICO)
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Journal of Neuromuscular Diseases
- ISSN: 2214-3599
- Volume/Número/Paginação/Ano: v. 1, n. 2, p. 169-179, Sept. 2014
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: bronze
-
ABNT
OLIVEIRA, Jorge et al. Reviewing large LAMA2 deletions and duplications in congenital muscular dystrophy patients. Journal of Neuromuscular Diseases, v. 1, n. 2, p. 169-179, 2014Tradução . . Disponível em: https://doi.org/10.3233/JND-140031. Acesso em: 12 maio 2024. -
APA
Oliveira, J., Gonçalves, A., Oliveira, M. E., Fineza, I., Pavanello, R. C. M., Vainzof, M., et al. (2014). Reviewing large LAMA2 deletions and duplications in congenital muscular dystrophy patients. Journal of Neuromuscular Diseases, 1( 2), 169-179. doi:10.3233/JND-140031 -
NLM
Oliveira J, Gonçalves A, Oliveira ME, Fineza I, Pavanello RCM, Vainzof M, Bonze-da-Rocha E, Santos R, Sousa M. Reviewing large LAMA2 deletions and duplications in congenital muscular dystrophy patients [Internet]. Journal of Neuromuscular Diseases. 2014 ; 1( 2): 169-179.[citado 2024 maio 12 ] Available from: https://doi.org/10.3233/JND-140031 -
Vancouver
Oliveira J, Gonçalves A, Oliveira ME, Fineza I, Pavanello RCM, Vainzof M, Bonze-da-Rocha E, Santos R, Sousa M. Reviewing large LAMA2 deletions and duplications in congenital muscular dystrophy patients [Internet]. Journal of Neuromuscular Diseases. 2014 ; 1( 2): 169-179.[citado 2024 maio 12 ] Available from: https://doi.org/10.3233/JND-140031 - 233rd ENMC International Workshop: Clinical Trial Readiness for Calpainopathies, Naarden, The Netherlands, 15–17 September 2017
- Behavioral responses in animal model of congenital muscular dystrophy 1D
- Effects of steroid hormones on myostatin expression and on genes of muscle regeneration pathway
- Estudo da atividade de quatro enzimas em tecido muscular de heterozigotas certas e afetadas por distrofias musculares progressivas: correlação com achados histológicos
- The contribution of muscle protein analysis in the diagnosis of genetic myopathies and in the understanding of the organization and maintenance of muscle fiber integrity
- Achados histológicos em biópsia muscular de eqüino com alterações neuromusculares
- Therapeutic potential of murine mesenchymal stem cells (MSC) from adipose tissue in the treatment of muscular dystrophy in the new double mutant mouse model for the genes dystrophin and large
- The mdx/SJL mouse: a new double mutant model for neuromuscular disorders with mutations in the dystrophin and dysferlin genes
- Heterozygous mutations in putative glycosyltransferase modulating the severity of the phenotype of muscular dystrophies
- Consensus statement on standard of care for congenital myopathies
Informações sobre o DOI: 10.3233/JND-140031 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
