LMX1B mutations cause hereditary FSGS without extrarenal involvement.

MLA

Boyer, Olivia, et al. “LMX1B Mutations Cause Hereditary FSGS without Extrarenal Involvement.” Journal of the American Society of Nephrology : JASN, vol. 24, no. 8, July 2013, pp. 1216–22. EBSCOhost, https://doi.org/10.1681/ASN.2013020171.

APA

Boyer, O., Woerner, S., Yang, F., Oakeley, E. J., Linghu, B., Gribouval, O., Tête, M.-J., Duca, J. S., Klickstein, L., Damask, A. J., Szustakowski, J. D., Heibel, F., Matignon, M., Baudouin, V., Chantrel, F., Champigneulle, J., Martin, L., Nitschké, P., Gubler, M.-C., … Antignac, C. (2013). LMX1B mutations cause hereditary FSGS without extrarenal involvement. Journal of the American Society of Nephrology : JASN, 24(8), 1216–1222. https://doi.org/10.1681/ASN.2013020171

Chicago

Boyer, Olivia, Stéphanie Woerner, Fan Yang, Edward J Oakeley, Bolan Linghu, Olivier Gribouval, Marie-Josèphe Tête, et al. 2013. “LMX1B Mutations Cause Hereditary FSGS without Extrarenal Involvement.” Journal of the American Society of Nephrology : JASN 24 (8): 1216–22. doi:10.1681/ASN.2013020171.