Cite
A novel CRX mutation by whole-exome sequencing in an autosomal dominant cone-rod dystrophy pedigree
MLA
Qin-Kang Lu, et al. “A Novel CRX Mutation by Whole-Exome Sequencing in an Autosomal Dominant Cone-Rod Dystrophy Pedigree.” International Journal of Ophthalmology, vol. 8, no. 6, Dec. 2015, pp. 1112–17. EBSCOhost, https://doi.org/10.3980/j.issn.2222-3959.2015.06.06.
APA
Qin-Kang Lu, Na Zhao, Ya-Su Lv, Wei-Kun Gong, Hui-Yun Wang, Qi-Hu Tong, Xiao-Ming Lai, Rong-Rong Liu, Ming-Yan Fang, Jian-Guo Zhang, Zhen-Fang Du, & Xian-Ning Zhang. (2015). A novel CRX mutation by whole-exome sequencing in an autosomal dominant cone-rod dystrophy pedigree. International Journal of Ophthalmology, 8(6), 1112–1117. https://doi.org/10.3980/j.issn.2222-3959.2015.06.06
Chicago
Qin-Kang Lu, Na Zhao, Ya-Su Lv, Wei-Kun Gong, Hui-Yun Wang, Qi-Hu Tong, Xiao-Ming Lai, et al. 2015. “A Novel CRX Mutation by Whole-Exome Sequencing in an Autosomal Dominant Cone-Rod Dystrophy Pedigree.” International Journal of Ophthalmology 8 (6): 1112–17. doi:10.3980/j.issn.2222-3959.2015.06.06.