Autosomal dominant retinitis pigmentosa with incomplete penetrance due to an intronic mutation of the PRPF31 gene.

MLA

Ali-Nasser, Tahleel, et al. “Autosomal Dominant Retinitis Pigmentosa with Incomplete Penetrance Due to an Intronic Mutation of the PRPF31 Gene.” Molecular Vision, vol. 28, Oct. 2022, pp. 359–68. 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=36338669&authtype=sso&custid=ns315887.

APA

Ali-Nasser, T., Zayit-Soudry, S., Banin, E., Sharon, D., & Ben-Yosef, T. (2022). Autosomal dominant retinitis pigmentosa with incomplete penetrance due to an intronic mutation of the PRPF31 gene. Molecular Vision, 28, 359–368.

Chicago

Ali-Nasser, Tahleel, Shiri Zayit-Soudry, Eyal Banin, Dror Sharon, and Tamar Ben-Yosef. 2022. “Autosomal Dominant Retinitis Pigmentosa with Incomplete Penetrance Due to an Intronic Mutation of the PRPF31 Gene.” Molecular Vision 28 (October): 359–68. 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=36338669&authtype=sso&custid=ns315887.