Cite
A Novel Small Insertion Mutation, C.1030_1031ins (T) in α-Galactosidase A Leads to Renal Variant Fabry Disease.
MLA
Choi, Joon Seok, et al. “A Novel Small Insertion Mutation, C.1030_1031ins (T) in α-Galactosidase A Leads to Renal Variant Fabry Disease.” Renal Failure, vol. 34, no. 3, Apr. 2012, pp. 390–93. EBSCOhost, https://doi.org/10.3109/0886022X.2011.647300.
APA
Choi, J. S., Kim, C. S., Park, J. W., Bae, E. H., Ma, S. K., Choi, Y. D., Kim, G. H., Yoo, H. W., & Kim, S. W. (2012). A Novel Small Insertion Mutation, C.1030_1031ins (T) in α-Galactosidase A Leads to Renal Variant Fabry Disease. Renal Failure, 34(3), 390–393. https://doi.org/10.3109/0886022X.2011.647300
Chicago
Choi, Joon Seok, Chang Seong Kim, Jeong Woo Park, Eun Hui Bae, Seong Kwon Ma, Yoo Duk Choi, Gu Hwan Kim, Han Wook Yoo, and Soo Wan Kim. 2012. “A Novel Small Insertion Mutation, C.1030_1031ins (T) in α-Galactosidase A Leads to Renal Variant Fabry Disease.” Renal Failure 34 (3): 390–93. doi:10.3109/0886022X.2011.647300.