Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidade: IB
Subjects: DISTROFIA MUSCULAR, MUTAÇÃO GENÉTICA, MODELOS ANIMAIS DE DOENÇAS
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: 03 nov. 2024. , 2011APA
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.2011.06.841NLM
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 nov. 03 ] Available from: https://doi.org/10.1016/j.nmd.2011.06.841Vancouver
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 nov. 03 ] Available from: https://doi.org/10.1016/j.nmd.2011.06.841