Tran, V. K., Diep, Q. M., Zilong, Q., Phuong, L. T., Tran, H. A., Tung, N. V., . . . Hoang, N. H. (2023). Case Report: Novel rare mutation c.6353C > G in the ABCA12 gene causing harlequin ichthyosis identified by whole exome sequencing. Frontiers in Pediatrics, 11, . https://doi.org/10.60692/241xs-fa025
Chicago-Zitierstil (17. Ausg.)Tran, Van Khanh, et al. "Case Report: Novel Rare Mutation C.6353C > G in the ABCA12 Gene Causing Harlequin Ichthyosis Identified by Whole Exome Sequencing." Frontiers in Pediatrics 11 (2023). https://doi.org/10.60692/241xs-fa025.
MLA-Zitierstil (9. Ausg.)Tran, Van Khanh, et al. "Case Report: Novel Rare Mutation C.6353C > G in the ABCA12 Gene Causing Harlequin Ichthyosis Identified by Whole Exome Sequencing." Frontiers in Pediatrics, vol. 11, 2023, https://doi.org/10.60692/241xs-fa025.