THAO, D. H.; ANH, N. P.; MIYAKE, N.; HAI, N. V.; MATSUMOTO, N.; DUONG, N. T. Whole exome sequencing revealed a mutation in COL6A1 associated with ullrich congenital muscular dystrophy . Vietnam Journal of Biotechnology, [S. l.], v. 19, n. 2, p. 213–221, 2021. DOI: 10.15625/1811-4989/16157. Disponível em: https://vjs.ac.vn/index.php/vjbt/article/view/16157. Acesso em: 22 nov. 2024.