Cite
Revealing the function of a novel splice-site mutation of CHD7 in CHARGE syndrome
MLA
Asuman Koparir, et al. “Revealing the Function of a Novel Splice-Site Mutation of CHD7 in CHARGE Syndrome.” Gene, vol. 576, no. 2 Pt 2, June 2015. 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.....01209b9079fb73a1e7df26e0805c4bd0&authtype=sso&custid=ns315887.
APA
Asuman Koparir, Mustafa Ozen, Borum Sagong, Un-Kyung Kim, Adnan Yuksel, Mehmet Bugrahan Duz, Jae Young Choi, Mehmet Seven, Byeonghyeon Lee, & Kyu-Yup Lee. (2015). Revealing the function of a novel splice-site mutation of CHD7 in CHARGE syndrome. Gene, 576(2 Pt 2).
Chicago
Asuman Koparir, Mustafa Ozen, Borum Sagong, Un-Kyung Kim, Adnan Yuksel, Mehmet Bugrahan Duz, Jae Young Choi, Mehmet Seven, Byeonghyeon Lee, and Kyu-Yup Lee. 2015. “Revealing the Function of a Novel Splice-Site Mutation of CHD7 in CHARGE Syndrome.” Gene 576 (2 Pt 2). 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.....01209b9079fb73a1e7df26e0805c4bd0&authtype=sso&custid=ns315887.