Cite
AP1S2 is mutated in X-linked Dandy–Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome)
MLA
Diana Zelenika, et al. AP1S2 Is Mutated in X-Linked Dandy–Walker Malformation with Intellectual Disability, Basal Ganglia Disease and Seizures (Pettigrew Syndrome). June 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.doi.dedup.....e30d813b515aefe09d9848529eeb7cd8&authtype=sso&custid=ns315887.
APA
Diana Zelenika, Nadine Girard, David H. Ledbetter, Pierre Cacciagli, Laurent Villard, William B. Dobyns, Nicolas Lévy, Mark Lathrop, Jean-Pierre Desvignes, & Marc Delepine. (2013). AP1S2 is mutated in X-linked Dandy–Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome).
Chicago
Diana Zelenika, Nadine Girard, David H. Ledbetter, Pierre Cacciagli, Laurent Villard, William B. Dobyns, Nicolas Lévy, Mark Lathrop, Jean-Pierre Desvignes, and Marc Delepine. 2013. “AP1S2 Is Mutated in X-Linked Dandy–Walker Malformation with Intellectual Disability, Basal Ganglia Disease and Seizures (Pettigrew Syndrome),” June. 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.....e30d813b515aefe09d9848529eeb7cd8&authtype=sso&custid=ns315887.