Investigation of an inherited PCGF2: p.Pro65Leu mutation causing Turnpenny-Fry syndrome.

MLA

Qi, Ke-Yan, et al. “Investigation of an Inherited PCGF2: P.Pro65Leu Mutation Causing Turnpenny-Fry Syndrome.” American Journal of Translational Research, vol. 14, no. 8, Aug. 2022, pp. 5591–97. 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=36105049&authtype=sso&custid=ns315887.

APA

Qi, K.-Y., Shen, M., Yang, K., Yan, Y.-S., Wu, J., Wang, Y.-P., & Yin, C.-H. (2022). Investigation of an inherited PCGF2: p.Pro65Leu mutation causing Turnpenny-Fry syndrome. American Journal of Translational Research, 14(8), 5591–5597.

Chicago

Qi, Ke-Yan, Ming Shen, Kai Yang, You-Sheng Yan, Jue Wu, Yi-Peng Wang, and Cheng-Hong Yin. 2022. “Investigation of an Inherited PCGF2: P.Pro65Leu Mutation Causing Turnpenny-Fry Syndrome.” American Journal of Translational Research 14 (8): 5591–97. 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=36105049&authtype=sso&custid=ns315887.