Heterozygous mutations in putative glycosyltransferase modulating the severity of the phenotype of muscular dystrophies (2011)
- Authors:
- Autor USP: VAINZOF, MARIZ - IB
- Unidade: IB
- DOI: 10.1016/j.nmd.2011.06.841
- Subjects: DISTROFIA MUSCULAR; MUTAÇÃO GENÉTICA; MODELOS ANIMAIS DE DOENÇAS
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Neuromuscular Disorders
- ISSN: 0960-8966
- Volume/Número/Paginação/Ano: v. 21, n. 9-10, p. 666, res. P2.18, Oct. 2011
- Conference titles: International Congress of the World Muscle Society
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
MARTINS-MACHADO, P et al. Heterozygous mutations in putative glycosyltransferase modulating the severity of the phenotype of muscular dystrophies. Neuromuscular Disorders. Oxford: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2011.06.841. Acesso em: 18 abr. 2024. , 2011 -
APA
Martins-Machado, P., Yamamoto, L. U., Onofre-Oliveira, P., Ayub-Guerrieri, D., & Vainzof, M. (2011). Heterozygous mutations in putative glycosyltransferase modulating the severity of the phenotype of muscular dystrophies. Neuromuscular Disorders. Oxford: Instituto de Biociências, Universidade de São Paulo. doi:10.1016/j.nmd.2011.06.841 -
NLM
Martins-Machado P, Yamamoto LU, Onofre-Oliveira P, Ayub-Guerrieri D, Vainzof M. Heterozygous mutations in putative glycosyltransferase modulating the severity of the phenotype of muscular dystrophies [Internet]. Neuromuscular Disorders. 2011 ; 21( 9-10): 666.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1016/j.nmd.2011.06.841 -
Vancouver
Martins-Machado P, Yamamoto LU, Onofre-Oliveira P, Ayub-Guerrieri D, Vainzof M. Heterozygous mutations in putative glycosyltransferase modulating the severity of the phenotype of muscular dystrophies [Internet]. Neuromuscular Disorders. 2011 ; 21( 9-10): 666.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1016/j.nmd.2011.06.841 - Immune-mediated rippling muscle disease in a patient with treated hypothyroidism. [Carta]
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Informações sobre o DOI: 10.1016/j.nmd.2011.06.841 (Fonte: oaDOI API)
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