APA (7th ed.) Citation

C, B., PR, R., V, L., JM, C., T, G., C, L., . . . S, V. (2017). Deletions Overlapping VCAN Exon 8 Are New Molecular Defects for Wagner Disease. Human mutation, 38(1), 43. https://doi.org/10.1002/humu.23124

Chicago Style (17th ed.) Citation

C, Burin-des-Roziers, Rothschild PR, Layet V, Chen JM, Ghiotti T, Leroux C, Cremers FP, Brézin AP, and Valleix S. "Deletions Overlapping VCAN Exon 8 Are New Molecular Defects for Wagner Disease." Human Mutation 38, no. 1 (2017): 43. https://doi.org/10.1002/humu.23124.

MLA (9th ed.) Citation

C, Burin-des-Roziers, et al. "Deletions Overlapping VCAN Exon 8 Are New Molecular Defects for Wagner Disease." Human Mutation, vol. 38, no. 1, 2017, p. 43, https://doi.org/10.1002/humu.23124.