APA aipamena

Esmailpour, T., Riazifar, H., Liu, L., Donkervoort, S., Huang, V. H., Madaan, S., . . . Huang, T. (2014). A splice donor mutation in NAA10 results in the dysregulation of the retinoic acid signaling pathway and causes Lenz microphthalmia syndrome. J Med Genet.

Chicago Style aipamena

Esmailpour, Taraneh, et al. "A Splice Donor Mutation in NAA10 Results in the Dysregulation of the Retinoic Acid Signaling Pathway and Causes Lenz Microphthalmia Syndrome." J Med Genet 2014.

MLA aipamena

Esmailpour, Taraneh, et al. "A Splice Donor Mutation in NAA10 Results in the Dysregulation of the Retinoic Acid Signaling Pathway and Causes Lenz Microphthalmia Syndrome." J Med Genet 2014.

Kontuz: berrikusi erreferentzia hauek erabili aurretik.