Coeli, F. B., Caldas Ferraz, L. F., Lemos-Marini, S. H. V. d., Pinto Rigatto, S. Z., Santoro Belangero, V. M., & Mello, M. P. d. [. (2008). Apparent Mineralocorticoid Excess Syndrome in a Brazilian Boy Caused by the Homozygous Missense Mutation p.R186C in the HSD11B2 Gene.
Referência de acordo com a norma ChicagoCoeli, Fernanda Borchers, Lucio Fabio Caldas Ferraz, Sofia H. V. de Lemos-Marini, Sumara Zuanazi Pinto Rigatto, Vera Maria Santoro Belangero, e Maricilda Palandi de [UNIFESP] Mello. Apparent Mineralocorticoid Excess Syndrome in a Brazilian Boy Caused By the Homozygous Missense Mutation P.R186C in the HSD11B2 Gene. 2008.
Referência de acordo com a norma MLACoeli, Fernanda Borchers, et al. Apparent Mineralocorticoid Excess Syndrome in a Brazilian Boy Caused By the Homozygous Missense Mutation P.R186C in the HSD11B2 Gene. 2008.