Thao, D. H., Anh, N. P., Miyake, N., Hai, N. V., Matsumoto, N. and Duong, N. T. (2021) “Whole exome sequencing revealed a mutation in COL6A1 associated with ullrich congenital muscular dystrophy ”, Vietnam Journal of Biotechnology, 19(2), pp. 213–221. doi: 10.15625/1811-4989/16157.