Cite
Generation of a human iPSC line from a patient with an optic atrophy 'plus' phenotype due to a mutation in the OPA1 gene
MLA
Rafael Garesse, et al. “Generation of a Human IPSC Line from a Patient with an Optic Atrophy ‘plus’ Phenotype Due to a Mutation in the OPA1 Gene.” Stem Cell Research, vol. 16, no. 3, Mar. 2016. 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.....eddfa1173d3a550fb035610f8a0aaee0&authtype=sso&custid=ns315887.
APA
Rafael Garesse, Mario F. Fraga, Francisco Zurita-Díaz, Agustín F. Fernández, Ana Moreno-Izquierdo, Carmen Ayuso, M. Esther Gallardo, & Teresa Galera-Monge. (2016). Generation of a human iPSC line from a patient with an optic atrophy “plus” phenotype due to a mutation in the OPA1 gene. Stem Cell Research, 16(3).
Chicago
Rafael Garesse, Mario F. Fraga, Francisco Zurita-Díaz, Agustín F. Fernández, Ana Moreno-Izquierdo, Carmen Ayuso, M. Esther Gallardo, and Teresa Galera-Monge. 2016. “Generation of a Human IPSC Line from a Patient with an Optic Atrophy ‘plus’ Phenotype Due to a Mutation in the OPA1 Gene.” Stem Cell Research 16 (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=edsair&AN=edsair.doi.dedup.....eddfa1173d3a550fb035610f8a0aaee0&authtype=sso&custid=ns315887.