SMC2, encoding a core component of the condensin complex, is mutated in Hallermann-Streiff syndrome: a condensinopathy revelation

MLA

Diab, Farah, et al. SMC2, Encoding a Core Component of the Condensin Complex, Is Mutated in Hallermann-Streiff Syndrome: A Condensinopathy Revelation. Jan. 2019. 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.dedup.wf.001..b11f1def607e42ac2461eb105c16ce63&authtype=sso&custid=ns315887.

APA

Diab, F., Watrin, E., Li, Y., Yigit, G., & Wollnik, B. (2019). SMC2, encoding a core component of the condensin complex, is mutated in Hallermann-Streiff syndrome: a condensinopathy revelation.

Chicago

Diab, Farah, Erwan Watrin, Yun Li, Gökhan Yigit, and Bernd Wollnik. 2019. “SMC2, Encoding a Core Component of the Condensin Complex, Is Mutated in Hallermann-Streiff Syndrome: A Condensinopathy Revelation,” January. 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.dedup.wf.001..b11f1def607e42ac2461eb105c16ce63&authtype=sso&custid=ns315887.