Comprehensive registration of DNA sequence variants associated with inherited retinal diseases in Leiden Open Variation Databases

MLA

Cremers, F. P. M., et al. “Comprehensive Registration of DNA Sequence Variants Associated with Inherited Retinal Diseases in Leiden Open Variation Databases.” Human Mutation, 2014. 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.on1284015423&authtype=sso&custid=ns315887.

APA

Cremers, F. P. M., Dunnen, J. T. den, Ajmal, M., Hussain, A., Preising, M. N., Daiger, S. P., & Qamar, R. (2014). Comprehensive registration of DNA sequence variants associated with inherited retinal diseases in Leiden Open Variation Databases. Human Mutation.

Chicago

Cremers, F.P.M., J.T. den Dunnen, M. Ajmal, A. Hussain, M.N. Preising, S.P. Daiger, and R. Qamar. 2014. “Comprehensive Registration of DNA Sequence Variants Associated with Inherited Retinal Diseases in Leiden Open Variation Databases.” Human Mutation. 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.on1284015423&authtype=sso&custid=ns315887.