Cite
Detailed Clinical Phenotype and Molecular Genetic Findings in CLN3-Associated Isolated Retinal Degeneration.
MLA
Ku, Cristy A., et al. “Detailed Clinical Phenotype and Molecular Genetic Findings in CLN3-Associated Isolated Retinal Degeneration.” JAMA Ophthalmology, 2017. 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=edsoai&AN=edsoai.on1287427457&authtype=sso&custid=ns315887.
APA
Ku, C. A., Ku, C. A., Hull, S., Arno, G., Vincent, A., Carss, K., Kayton, R., Weeks, D., Anderson, G. W., Geraets, R., Parker, C., Pearce, D. A., Michaelides, M., MacLaren, R. E., Robson, A. G., Holder, G. E., Heon, E., Raymond, F. L., Moore, A. T., … Pennesi, M. E. (2017). Detailed Clinical Phenotype and Molecular Genetic Findings in CLN3-Associated Isolated Retinal Degeneration. JAMA Ophthalmology.
Chicago
Ku, Cristy A, Cristy A Ku, Sarah Hull, Gavin Arno, Ajoy Vincent, Keren Carss, Robert Kayton, et al. 2017. “Detailed Clinical Phenotype and Molecular Genetic Findings in CLN3-Associated Isolated Retinal Degeneration.” JAMA Ophthalmology. 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=edsoai&AN=edsoai.on1287427457&authtype=sso&custid=ns315887.