Cite
A comprehensive search for mutations in the PKD1 and PKD2 in Japanese subjects with autosomal dominant polycystic kidney disease
MLA
M, Kurashige, et al. “A Comprehensive Search for Mutations in the PKD1 and PKD2 in Japanese Subjects with Autosomal Dominant Polycystic Kidney Disease.” Clinical Genetics, vol. 87, no. 3, Dec. 2013. 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..........37b5cbd9660f3c7392bd4144b16bcb6e&authtype=sso&custid=ns315887.
APA
M, K., K, H., M, I., T, U., Y, K., T, H., T, H., T, Y., & S, M. (2013). A comprehensive search for mutations in the PKD1 and PKD2 in Japanese subjects with autosomal dominant polycystic kidney disease. Clinical Genetics, 87(3).
Chicago
M, Kurashige, Hanaoka K, Imamura M, Udagawa T, Kawaguchi Y, Hasegawa T, Hosoya T, Yokoo T, and Maeda S. 2013. “A Comprehensive Search for Mutations in the PKD1 and PKD2 in Japanese Subjects with Autosomal Dominant Polycystic Kidney Disease.” Clinical Genetics 87 (3). 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..........37b5cbd9660f3c7392bd4144b16bcb6e&authtype=sso&custid=ns315887.