Novel human pathological mutations. Gene symbol: MECP2. Disease: Rett Syndrome.

MLA

Khajuria, Rajni, et al. “Novel Human Pathological Mutations. Gene Symbol: MECP2. Disease: Rett Syndrome.” Human Genetics, vol. 127, no. 1, Jan. 2010, p. 117. 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=20108429&authtype=sso&custid=ns315887.

APA

Khajuria, R., Sapra, S., Ghosh, M., Gupta, N., Gulati, S., Kalra, V., & Kabra, M. (2010). Novel human pathological mutations. Gene symbol: MECP2. Disease: Rett Syndrome. Human Genetics, 127(1), 117.

Chicago

Khajuria, Rajni, Savita Sapra, Manju Ghosh, Neerja Gupta, Sheffali Gulati, Veena Kalra, and Madhulika Kabra. 2010. “Novel Human Pathological Mutations. Gene Symbol: MECP2. Disease: Rett Syndrome.” Human Genetics 127 (1): 117. 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=20108429&authtype=sso&custid=ns315887.