A missense mutation at the [Gamma]42 secretase site in APP points to an essential role for N-truncated A[Beta]42 in Alzheimer's disease

MLA

Van Broeckhoven, C., et al. “A Missense Mutation at the [Gamma]42 Secretase Site in APP Points to an Essential Role for N-Truncated A[Beta]42 in Alzheimer’s Disease.” American Journal of Human Genetics, vol. 67, no. 4, Oct. 2000, p. 407. 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=edsggo&AN=edsgcl.66671158&authtype=sso&custid=ns315887.

APA

Van Broeckhoven, C., Kumar-Singh, S., De Jonghe, C., Cruts, M., Kleinert, R., Wang, R., Mercken, M. V. H., Lofgren, A., Vanmechelen, E., & Kroisel, P. M. (2000). A missense mutation at the [Gamma]42 secretase site in APP points to an essential role for N-truncated A[Beta]42 in Alzheimer’s disease. American Journal of Human Genetics, 67(4), 407.

Chicago

Van Broeckhoven, C., S. Kumar-Singh, C. De Jonghe, M. Cruts, R. Kleinert, R. Wang, M. Vanderstichele, H. Mercken, A. Lofgren, E. Vanmechelen, and P.M. Kroisel. 2000. “A Missense Mutation at the [Gamma]42 Secretase Site in APP Points to an Essential Role for N-Truncated A[Beta]42 in Alzheimer’s Disease.” American Journal of Human Genetics 67 (4): 407. 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=edsggo&AN=edsgcl.66671158&authtype=sso&custid=ns315887.