Cite
Clinical Utility Gene Card for: Autosomal dominant myotonia congenita (Thomsen Disease)
MLA
Coote, D. J., et al. “Clinical Utility Gene Card for: Autosomal Dominant Myotonia Congenita (Thomsen Disease).” Coote, D.J., Davis, M.R., Cabrera, M., Needham, M. <, 2018. 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.on1044728188&authtype=sso&custid=ns315887.
APA
Coote, D. J., Davis, M. R., Cabrera, M., Needham, M., Laing, N. G., & Nowak, K. J. (2018). Clinical Utility Gene Card for: Autosomal dominant myotonia congenita (Thomsen Disease). Coote, D.J., Davis, M.R., Cabrera, M., Needham, M. <.
Chicago
Coote, D.J., M.R. Davis, M. Cabrera, M. Needham, N.G. Laing, and K.J. Nowak. 2018. “Clinical Utility Gene Card for: Autosomal Dominant Myotonia Congenita (Thomsen Disease).” Coote, D.J., Davis, M.R., Cabrera, M., Needham, M. <. 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.on1044728188&authtype=sso&custid=ns315887.