Exome sequencing identified null mutations in LOXL3 associated with early-onset high myopia.

MLA

Jiali Li, et al. “Exome Sequencing Identified Null Mutations in LOXL3 Associated with Early-Onset High Myopia.” Molecular Vision, vol. 22, Dec. 2016, pp. 1–7. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edb&AN=124085574&authtype=sso&custid=ns315887.

APA

Jiali Li, Bei Gao, Xueshan Xiao, Shiqiang Li, Xiaoyun Jia, Wenmin Sun, Xiangming Guo, & Qingjiong Zhang. (2016). Exome sequencing identified null mutations in LOXL3 associated with early-onset high myopia. Molecular Vision, 22, 1–7.

Chicago

Jiali Li, Bei Gao, Xueshan Xiao, Shiqiang Li, Xiaoyun Jia, Wenmin Sun, Xiangming Guo, and Qingjiong Zhang. 2016. “Exome Sequencing Identified Null Mutations in LOXL3 Associated with Early-Onset High Myopia.” Molecular Vision 22 (December): 1–7. http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edb&AN=124085574&authtype=sso&custid=ns315887.