Autosomal dominant hereditary spastic paraplegia: DHPLC-based mutation analysis of SPG4 reveals eleven novel mutations.

MLA

Patrono, Clarice, et al. Autosomal Dominant Hereditary Spastic Paraplegia: DHPLC-Based Mutation Analysis of SPG4 Reveals Eleven Novel Mutations. 2005. 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.on1104979579&authtype=sso&custid=ns315887.

APA

Patrono, C., Scarano, V., Cricchi, F., Melone, M., Chiriaco, M., Napolitano, A., Malandrini, A., De Michelis, G., Petrozzi, L., Girlaldi, C., Santoro, L., Servidei, S., Casali, C., Filla, A., Santorelli, F. M., & Servidei, S. (ORCID:0000-0001-8478-2799). (2005). Autosomal dominant hereditary spastic paraplegia: DHPLC-based mutation analysis of SPG4 reveals eleven novel mutations.

Chicago

Patrono, Clarice, Valentina Scarano, Federica Cricchi, Mariarosa Melone, Maria Chiriaco, Alessandro Napolitano, Alessandro Malandrini, et al. 2005. “Autosomal Dominant Hereditary Spastic Paraplegia: DHPLC-Based Mutation Analysis of SPG4 Reveals Eleven Novel Mutations.” 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.on1104979579&authtype=sso&custid=ns315887.