Cite
A novel missense mutation of RPGR identified from retinitis pigmentosa affects splicing of the ORF15 region and causes loss of transcript heterogeneity.
MLA
Liu, Yan-Shan, et al. “A Novel Missense Mutation of RPGR Identified from Retinitis Pigmentosa Affects Splicing of the ORF15 Region and Causes Loss of Transcript Heterogeneity.” Biochemical & Biophysical Research Communications, vol. 531, no. 2, Oct. 2020, pp. 172–79. EBSCOhost, https://doi.org/10.1016/j.bbrc.2020.06.109.
APA
Liu, Y.-S., Pan, J.-Q., Wan, J.-F., Ren, C.-Y., Xu, Z.-H., Pan, X.-B., Gao, R.-N., Liu, S.-Q., Zhang, J.-L., Yao, Q.-H., Wang, J.-H., Li, E.-M., Rao, J.-H., Hou, P., & Chen, J.-H. (2020). A novel missense mutation of RPGR identified from retinitis pigmentosa affects splicing of the ORF15 region and causes loss of transcript heterogeneity. Biochemical & Biophysical Research Communications, 531(2), 172–179. https://doi.org/10.1016/j.bbrc.2020.06.109
Chicago
Liu, Yan-Shan, Jia-Qi Pan, Ji-Feng Wan, Chun-Yan Ren, Zhou-Heng Xu, Xu-Bin Pan, Ruo-Nan Gao, et al. 2020. “A Novel Missense Mutation of RPGR Identified from Retinitis Pigmentosa Affects Splicing of the ORF15 Region and Causes Loss of Transcript Heterogeneity.” Biochemical & Biophysical Research Communications 531 (2): 172–79. doi:10.1016/j.bbrc.2020.06.109.