Cite
Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia
MLA
Yuji Nagayama, et al. “Malfunction of Nuclease ERCC1-XPF Results in Diverse Clinical Manifestations and Causes Cockayne Syndrome, Xeroderma Pigmentosum, and Fanconi Anemia.” American Journal of Human Genetics, vol. 92, no. 5, Nov. 2012. 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=edsair&AN=edsair.doi.dedup.....2b9b8a18a15384837c007645f43c9f64&authtype=sso&custid=ns315887.
APA
Yuji Nagayama, Daniela T. Pilz, Kensaku Sasaki, Susan O. Lewin, Guo Chaowan, Akiyoshi Hirano, Danielle Greenblatt, Norisato Mitsutake, Tao-Sheng Li, Alan R. Lehmann, Jonathan F. Wing, Robert Sarkany, Atsushi Utani, Shunichi Yamashita, Hiva Fassihi, D.H. McGIBBON, Tomoo Ogi, Tiziana Nardo, Miria Stefanini, … Yuka Nakazawa. (2012). Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia. American Journal of Human Genetics, 92(5).
Chicago
Yuji Nagayama, Daniela T. Pilz, Kensaku Sasaki, Susan O. Lewin, Guo Chaowan, Akiyoshi Hirano, Danielle Greenblatt, et al. 2012. “Malfunction of Nuclease ERCC1-XPF Results in Diverse Clinical Manifestations and Causes Cockayne Syndrome, Xeroderma Pigmentosum, and Fanconi Anemia.” American Journal of Human Genetics 92 (5). 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=edsair&AN=edsair.doi.dedup.....2b9b8a18a15384837c007645f43c9f64&authtype=sso&custid=ns315887.