Spinal cord atrophy in triple A syndrome associated with a novel compound heterozygous mutation.

MLA

Kunte, Hagen, et al. “Spinal Cord Atrophy in Triple A Syndrome Associated with a Novel Compound Heterozygous Mutation.” Neuro Endocrinology Letters, vol. 31, no. 3, 2010, pp. 301–03. 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=20588230&authtype=sso&custid=ns315887.

APA

Kunte, H., Trendelenburg, G., Matzen, J., Ventz, M., Kornak, U., & Harms, L. (2010). Spinal cord atrophy in triple A syndrome associated with a novel compound heterozygous mutation. Neuro Endocrinology Letters, 31(3), 301–303.

Chicago

Kunte, Hagen, George Trendelenburg, Julia Matzen, Manfred Ventz, Uwe Kornak, and Lutz Harms. 2010. “Spinal Cord Atrophy in Triple A Syndrome Associated with a Novel Compound Heterozygous Mutation.” Neuro Endocrinology Letters 31 (3): 301–3. 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=20588230&authtype=sso&custid=ns315887.