A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effect

MLA

Di Maria, E., et al. “A Novel Mutation of GDAP1 Associated with Charcot-Marie-Tooth Disease in Three Italian Families: Evidence for a Founder Effect.” Journal of Neurology, Neurosurgery and Psychiatry, vol. 75, no. 10, Oct. 2004, p. 1495. 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.134742708&authtype=sso&custid=ns315887.

APA

Di Maria, E., Gulli, R., Balestra, P., Cassandrini, D., Pigullo, S., Doria-Lamba, L., Bado, M., Schenone, A., Ajmar, F., Mandich, P., & Bellone, E. (2004). A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effect. Journal of Neurology, Neurosurgery and Psychiatry, 75(10), 1495.

Chicago

Di Maria, E., R. Gulli, P. Balestra, D. Cassandrini, S. Pigullo, L. Doria-Lamba, M. Bado, et al. 2004. “A Novel Mutation of GDAP1 Associated with Charcot-Marie-Tooth Disease in Three Italian Families: Evidence for a Founder Effect.” Journal of Neurology, Neurosurgery and Psychiatry 75 (10): 1495. 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.134742708&authtype=sso&custid=ns315887.