NPHS2 mutations account for only 15% of nephrotic syndrome cases von Guaragna, Mara Sanches, Lutaif, Anna Cristina G B, Piveta, Cristiane S C, Souza, Marcela L, de Souza, Suéllen R, Henriques, Taciane B, Maciel-Guerra, Andréa T, Belangero, Vera M S, Guerra-Junior, Gil, De Mello, Maricilda P

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NPHS2 Mutations: A Closer Look to Latin American Countries von Guerra-Júnior, Gil, Belangero, Vera Maria Santoro, Maciel-Guerra, Andréa Trevas, Lutaif, Anna Cristina G. B., Guaragna, Mara Sanches, de Mello, Maricilda Palandi

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NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described von Guaragna, Mara S., Cleto, Thaís Lira, Souza, Marcela Lopes, Lutaif, Anna Cristina G.B., de Castro, Luiz Cláudio Gonçalves, Penido, Maria Goretti Moreira Guimarães, Maciel-Guerra, Andréa T., Belangero, Vera M.S., Guerra-Junior, Gil, De Mello, Maricilda P.

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Two distinct WT1 mutations identified in patients and relatives with isolated nephrotic proteinuria von Guaragna, Mara S., Lutaif, Anna Cristina G.B., Piveta, Cristiane S.C., Belangero, Vera M.S., Maciel-Guerra, Andréa T., Guerra-Junior, Gil, De Mello, Maricilda P.

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