Cite
A Novel c.676_677insG PHOX2B Mutation in Congenital Central Hypoventilation Syndrome
MLA
Han Daxiong, et al. “A Novel c.676_677insG PHOX2B Mutation in Congenital Central Hypoventilation Syndrome.” Journal of Clinical Sleep Medicine, vol. 15, Mar. 2019, pp. 509–13. 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...........7b7fd129d7ca7e64359f113d02e67784&authtype=sso&custid=ns315887.
APA
Han Daxiong, Qiwei Guo, Yulin Zhou, Zengge Wang, Guo-Dong Ye, Chen Weiwei, Xinzhu Lin, Yu Jiang, Xu Jianxiong, Chen Maoli, & Yang Yanyan. (2019). A Novel c.676_677insG PHOX2B Mutation in Congenital Central Hypoventilation Syndrome. Journal of Clinical Sleep Medicine, 15, 509–513.
Chicago
Han Daxiong, Qiwei Guo, Yulin Zhou, Zengge Wang, Guo-Dong Ye, Chen Weiwei, Xinzhu Lin, et al. 2019. “A Novel c.676_677insG PHOX2B Mutation in Congenital Central Hypoventilation Syndrome.” Journal of Clinical Sleep Medicine 15 (March): 509–13. 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...........7b7fd129d7ca7e64359f113d02e67784&authtype=sso&custid=ns315887.