Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy

MLA

McMillan, Hj, et al. Recessive Mutations in ATP8A2 Cause Severe Hypotonia, Cognitive Impairment, Hyperkinetic Movement Disorders and Progressive Optic Atrophy. 2018. 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=edsoai&AN=edsoai.on1315678942&authtype=sso&custid=ns315887.

APA

McMillan, H., Telegrafi, A., Singleton, A., Cho, M., Lelli, D., Lynn, F., Griffin, J., Asamoah, A., Rinne, T., Erasmus, C., Koolen, D., Haaxma, C., Keren, B., Doummar, D., Mignot, C., Thompson, I., Velsher, L., Dehghani, M., Mehrjardi, M., … Yoon, G. (2018). Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy.

Chicago

McMillan, Hj, A Telegrafi, A Singleton, Mt Cho, D Lelli, Fc Lynn, J Griffin, et al. 2018. “Recessive Mutations in ATP8A2 Cause Severe Hypotonia, Cognitive Impairment, Hyperkinetic Movement Disorders and Progressive Optic Atrophy.” 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=edsoai&AN=edsoai.on1315678942&authtype=sso&custid=ns315887.