1.Thao DH, Anh NP, Miyake N, Hai NV, Matsumoto N, Duong NT. Whole exome sequencing revealed a mutation in COL6A1 associated with ullrich congenital muscular dystrophy . Vietnam J. Biotechnol. [Internet]. 2021 Aug. 2 [cited 2026 Jan. 12];19(2):213-21. Available from: https://vjes.vast.vn/vjbt/article/view/16157