A deep intronic substitution in CNGB3 is one of the major causes of achromatopsia among Jewish patients.

MLA

Aweidah, Hamzah, et al. “A Deep Intronic Substitution in CNGB3 Is One of the Major Causes of Achromatopsia among Jewish Patients.” Molecular Vision, vol. 27, Sept. 2021, pp. 588–600. 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=cmedm&AN=34703197&authtype=sso&custid=ns315887.

APA

Aweidah, H., Salameh, M., Yahalom, C., Blumenfeld, A., Macarov, M., Weisschuh, N., Kohl, S., Banin, E., & Sharon, D. (2021). A deep intronic substitution in CNGB3 is one of the major causes of achromatopsia among Jewish patients. Molecular Vision, 27, 588–600.

Chicago

Aweidah, Hamzah, Manar Salameh, Claudia Yahalom, Anat Blumenfeld, Michal Macarov, Nicole Weisschuh, Susanne Kohl, Eyal Banin, and Dror Sharon. 2021. “A Deep Intronic Substitution in CNGB3 Is One of the Major Causes of Achromatopsia among Jewish Patients.” Molecular Vision 27 (September): 588–600. 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=cmedm&AN=34703197&authtype=sso&custid=ns315887.