W179R: a novel missense mutation in the peripherin/RDS gene in a family with autosomal dominant retinitis pigmentosa

MLA

C, Bareil, et al. “W179R: A Novel Missense Mutation in the Peripherin/RDS Gene in a Family with Autosomal Dominant Retinitis Pigmentosa.” Human Mutation, vol. 15, no. 6, June 2000. 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.pmid..........e4ecc276c0e34f4598b4200f164eb6c9&authtype=sso&custid=ns315887.

APA

C, B., V, D., B, A., J, D., C, H., & M, C. (2000). W179R: a novel missense mutation in the peripherin/RDS gene in a family with autosomal dominant retinitis pigmentosa. Human Mutation, 15(6).

Chicago

C, Bareil, Delague V, Arnaud B, Demaille J, Hamel C, and Claustres M. 2000. “W179R: A Novel Missense Mutation in the Peripherin/RDS Gene in a Family with Autosomal Dominant Retinitis Pigmentosa.” Human Mutation 15 (6). 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.pmid..........e4ecc276c0e34f4598b4200f164eb6c9&authtype=sso&custid=ns315887.