RET mutation p.S891A in a Chinese family with familial medullary thyroid carcinoma and associated cutaneous amyloidosis binding OSMR variant p.G513D.

MLA

Qi, Xiao-Ping, et al. “RET Mutation p.S891A in a Chinese Family with Familial Medullary Thyroid Carcinoma and Associated Cutaneous Amyloidosis Binding OSMR Variant p.G513D.” Oncotarget, vol. 6, no. 32, Oct. 2015, pp. 33993–4003. EBSCOhost, https://doi.org/10.18632/oncotarget.4992.

APA

Qi, X.-P., Zhao, J.-Q., Chen, Z.-G., Cao, J.-L., Du, J., Liu, N.-F., Li, F., Sheng, M., Fu, E., Guo, J., Jia, H., Zhang, Y.-M., & Ma, J.-M. (2015). RET mutation p.S891A in a Chinese family with familial medullary thyroid carcinoma and associated cutaneous amyloidosis binding OSMR variant p.G513D. Oncotarget, 6(32), 33993–34003. https://doi.org/10.18632/oncotarget.4992

Chicago

Qi, Xiao-Ping, Jian-Qiang Zhao, Zhen-Guang Chen, Jin-Lin Cao, Juan Du, Nai-Fang Liu, Feng Li, et al. 2015. “RET Mutation p.S891A in a Chinese Family with Familial Medullary Thyroid Carcinoma and Associated Cutaneous Amyloidosis Binding OSMR Variant p.G513D.” Oncotarget 6 (32): 33993–3. doi:10.18632/oncotarget.4992.