Severe congenital cutis laxa with cardiovascular manifestations due to homozygous deletions in ALDH18A1

MLA

Fischer, B., et al. “Severe Congenital Cutis Laxa with Cardiovascular Manifestations Due to Homozygous Deletions in ALDH18A1.” Molecular Genetics and Metabolism, 2014. 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.on1247302486&authtype=sso&custid=ns315887.

APA

Fischer, B., Callewaert, B., Schroter, P., Coucke, P. J., Schlack, C., Ott, C. E., Morroni, M., Homann, W., Mundlos, S., Morava, E., Ficcadenti, A., & Kornak, U. (2014). Severe congenital cutis laxa with cardiovascular manifestations due to homozygous deletions in ALDH18A1. Molecular Genetics and Metabolism.

Chicago

Fischer, B., B. Callewaert, P. Schroter, P.J. Coucke, C. Schlack, C.E. Ott, M. Morroni, et al. 2014. “Severe Congenital Cutis Laxa with Cardiovascular Manifestations Due to Homozygous Deletions in ALDH18A1.” Molecular Genetics and Metabolism. 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.on1247302486&authtype=sso&custid=ns315887.