APA aipamena

Guaragna, M. S., Lutaif, A. C. G., Piveta, C. S., Souza, M. L., de Souza, S. R., Henriques, T. B., . . . De Mello, M. P. (2015). NPHS2 mutations account for only 15 % of nephrotic syndrome cases. BMC Med Genet.

Chicago Style aipamena

Guaragna, Mara Sanches, et al. "NPHS2 Mutations Account for Only 15 % of Nephrotic Syndrome Cases." BMC Med Genet 2015.

MLA aipamena

Guaragna, Mara Sanches, et al. "NPHS2 Mutations Account for Only 15 % of Nephrotic Syndrome Cases." BMC Med Genet 2015.

Kontuz: berrikusi erreferentzia hauek erabili aurretik.