Disturbed copper transport in humans. Part 1: mutations of the ATP7A gene lead to Menkes disease and occipital horn syndrome.

MLA

Seidel, J., et al. “Disturbed Copper Transport in Humans. Part 1: Mutations of the ATP7A Gene Lead to Menkes Disease and Occipital Horn Syndrome.” Cellular and Molecular Biology (Noisy-Le-Grand, France), vol. 47 Online Pub, 2001, pp. OL141-OL148. 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=cmedm&AN=11936860&authtype=sso&custid=ns315887.

APA

Seidel, J., Møller, L. B., Mentzel, H. J., Kauf, E., Vogt, S., Patzer, S., Wollina, U., Zintl, F., & Horn, N. (2001). Disturbed copper transport in humans. Part 1: mutations of the ATP7A gene lead to Menkes disease and occipital horn syndrome. Cellular and Molecular Biology (Noisy-Le-Grand, France), 47 Online Pub, OL141-OL148.

Chicago

Seidel, J, L B Møller, H J Mentzel, E Kauf, S Vogt, S Patzer, U Wollina, F Zintl, and N Horn. 2001. “Disturbed Copper Transport in Humans. Part 1: Mutations of the ATP7A Gene Lead to Menkes Disease and Occipital Horn Syndrome.” Cellular and Molecular Biology (Noisy-Le-Grand, France) 47 Online Pub: OL141-OL148. 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=cmedm&AN=11936860&authtype=sso&custid=ns315887.