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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 2024 Jul. 25];19(2):213-21. Available from: https://vjs.ac.vn/index.php/vjbt/article/view/16157