Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease

MLA

Annie Lahoche, et al. “Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease.” Journal of the American Society of Nephrology, vol. 27, Mar. 2016, pp. 722–29. EBSCOhost, https://doi.org/10.1681/asn.2014101051.

APA

Annie Lahoche, Françoise Broux, Ferielle Louillet, Vincent Morinière, Olivia Boyer, Amélie Ryckenwaert, Hanitra Randrianaivo, Elodie Merieau, Said Lebbah, Stéphane Decramer, Marie-Pierre Audrézet, Djalila Mekahli, Sandrine Maestri, Laurence Heidet, Carine Abel, Christine Corbiere, Georges Deschênes, Claude Férec, Ines Ouertani, … Lucie Bessenay. (2016). Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease. Journal of the American Society of Nephrology, 27, 722–729. https://doi.org/10.1681/asn.2014101051

Chicago

Annie Lahoche, Françoise Broux, Ferielle Louillet, Vincent Morinière, Olivia Boyer, Amélie Ryckenwaert, Hanitra Randrianaivo, et al. 2016. “Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease.” Journal of the American Society of Nephrology 27 (March): 722–29. doi:10.1681/asn.2014101051.