[1]
D. H. Thao, N. P. Anh, N. Miyake, N. V. Hai, N. Matsumoto, and N. T. Duong, “Whole exome sequencing revealed a mutation in COL6A1 associated with ullrich congenital muscular dystrophy ”, Vietnam J. Biotechnol., vol. 19, no. 2, pp. 213–221, Aug. 2021.