A novel NGFB point mutation: a phenotype study of heterozygous patients

MLA

Minde, J., et al. “A Novel NGFB Point Mutation: A Phenotype Study of Heterozygous Patients.” Journal of Neurology, Neurosurgery and Psychiatry, vol. 80, no. 2, Feb. 2009, p. 188. 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.195615079&authtype=sso&custid=ns315887.

APA

Minde, J., Andersson, T., Fulford, M., Aguirre, M., Nennesmo, I., Remahl, I. N., Svensson, O., Holmberg, M., Toolanen, G., & Solders, G. (2009). A novel NGFB point mutation: a phenotype study of heterozygous patients. Journal of Neurology, Neurosurgery and Psychiatry, 80(2), 188.

Chicago

Minde, J., T. Andersson, M. Fulford, M. Aguirre, I. Nennesmo, I. Nilsson Remahl, O. Svensson, M. Holmberg, G. Toolanen, and G. Solders. 2009. “A Novel NGFB Point Mutation: A Phenotype Study of Heterozygous Patients.” Journal of Neurology, Neurosurgery and Psychiatry 80 (2): 188. 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.195615079&authtype=sso&custid=ns315887.