Cite
Mutations in Splicing Factor Genes Are a Major Cause of Autosomal Dominant Retinitis Pigmentosa in Belgian Families
MLA
Fanny Depasse, et al. “Mutations in Splicing Factor Genes Are a Major Cause of Autosomal Dominant Retinitis Pigmentosa in Belgian Families.” PLoS ONE, vol. 12, no. 1, Jan. 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=edsair&AN=edsair.doi.dedup.....3483f5dc85d6ddc874768826cb0ba5bc&authtype=sso&custid=ns315887.
APA
Fanny Depasse, Elfride De Baere, Bart P. Leroy, Charlotte Claes, Ingele Casteels, Erik Fransén, Caroline Van Cauwenbergh, Dimitri Roels, Thomy de Ravel, Frauke Coppieters, Julie De Zaeytijd, Sarah De Jaegere, Sophie Walraedt, Guy Van Camp, & Helena Flipts. (2017). Mutations in Splicing Factor Genes Are a Major Cause of Autosomal Dominant Retinitis Pigmentosa in Belgian Families. PLoS ONE, 12(1).
Chicago
Fanny Depasse, Elfride De Baere, Bart P. Leroy, Charlotte Claes, Ingele Casteels, Erik Fransén, Caroline Van Cauwenbergh, et al. 2017. “Mutations in Splicing Factor Genes Are a Major Cause of Autosomal Dominant Retinitis Pigmentosa in Belgian Families.” PLoS ONE 12 (1). 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=edsair&AN=edsair.doi.dedup.....3483f5dc85d6ddc874768826cb0ba5bc&authtype=sso&custid=ns315887.