Cite
A novel form of cell type-specific partial IFN-γR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon
MLA
Christophe Lamaze, et al. “A Novel Form of Cell Type-Specific Partial IFN-ΓR1 Deficiency Caused by a Germ Line Mutation of the IFNGR1 Initiation Codon.” Human Molecular Genetics, vol. 19, Oct. 2009, pp. 434–44. 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.....dfe6c488d6413ca6ea9c8094df1754ba&authtype=sso&custid=ns315887.
APA
Christophe Lamaze, Guillaume Vogt, Ariane Chapgier, Jacqueline Feinberg, Matti Korppi, Petra Moilanen, Carolina Prando, Stéphanie Boisson-Dupuis, Jean-Laurent Casanova, Mikko Arola, Anne Puel, Jacinta Bustamante, Xiao-Fei Kong, Anny Fortin, Xinxin Zhang, Ulla M. Pihkala-Saarinen, Laurent Abel, & Pauline Gonnord. (2009). A novel form of cell type-specific partial IFN-γR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon. Human Molecular Genetics, 19, 434–444.
Chicago
Christophe Lamaze, Guillaume Vogt, Ariane Chapgier, Jacqueline Feinberg, Matti Korppi, Petra Moilanen, Carolina Prando, et al. 2009. “A Novel Form of Cell Type-Specific Partial IFN-ΓR1 Deficiency Caused by a Germ Line Mutation of the IFNGR1 Initiation Codon.” Human Molecular Genetics 19 (October): 434–44. 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.....dfe6c488d6413ca6ea9c8094df1754ba&authtype=sso&custid=ns315887.