Loss of nuclear UBE3A activity is the predominant cause of Angelman syndrome in individuals carrying UBE3A missense mutations

MLA

A. Mattijs Punt, et al. “Loss of Nuclear UBE3A Activity Is the Predominant Cause of Angelman Syndrome in Individuals Carrying UBE3A Missense Mutations.” Human Molecular Genetics, vol. 30, no. 6, Mar. 2021, pp. 430–42. 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.....f9718602a9b38a7e220c2b1b5f796291&authtype=sso&custid=ns315887.

APA

A. Mattijs Punt, Janny van den Burg, Ilona J. de Graaf, Mark Williams, Helen Heussler, Ype Elgersma, Stijn N V Bossuyt, & Ben Distel. (2021). Loss of nuclear UBE3A activity is the predominant cause of Angelman syndrome in individuals carrying UBE3A missense mutations. Human Molecular Genetics, 30(6), 430–442.

Chicago

A. Mattijs Punt, Janny van den Burg, Ilona J. de Graaf, Mark Williams, Helen Heussler, Ype Elgersma, Stijn N V Bossuyt, and Ben Distel. 2021. “Loss of Nuclear UBE3A Activity Is the Predominant Cause of Angelman Syndrome in Individuals Carrying UBE3A Missense Mutations.” Human Molecular Genetics 30 (6): 430–42. 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.....f9718602a9b38a7e220c2b1b5f796291&authtype=sso&custid=ns315887.