A novel ABHD5 mutation in two Chanarin Dorfman siblings with severe and heterogeneous clinical phenotype

MLA

Elsayed, S. M., et al. A Novel ABHD5 Mutation in Two Chanarin Dorfman Siblings with Severe and Heterogeneous Clinical Phenotype. 2022. 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.on1355229275&authtype=sso&custid=ns315887.

APA

Elsayed, S. M., Torre, E., Tavian, D., Moro, L., Angelini, C., Abdel Ghaffar, T. Y., Zalata, K., Fahmy, E. E., Missaglia, S., Torre E. (ORCID:0000-0001-6754-2611), Tavian D. (ORCID:0000-0003-3333-0068), & Missaglia S. (ORCID:0000-0001-6551-6698). (2022). A novel ABHD5 mutation in two Chanarin Dorfman siblings with severe and heterogeneous clinical phenotype.

Chicago

Elsayed, S. M., Enza Torre, Daniela Tavian, L. Moro, C. Angelini, T. Y. Abdel Ghaffar, K. Zalata, et al. 2022. “A Novel ABHD5 Mutation in Two Chanarin Dorfman Siblings with Severe and Heterogeneous Clinical Phenotype.” 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.on1355229275&authtype=sso&custid=ns315887.