NPHS2 mutations account for only 15 % of nephrotic syndrome cases

por Guaragna, Mara Sanches, Lutaif, Anna Cristina GB, Piveta, Cristiane SC, Souza, Marcela L., de Souza, Suéllen R., Henriques, Taciane B., Maciel-Guerra, Andréa T., Belangero, Vera MS, Guerra-Junior, Gil, De Mello, Maricilda P.
Publicado 2015

Brazilian Network of Pediatric Nephrotic Syndrome (REBRASNI)

por Feltran, Luciana S., Watanabe, Andreia, Guaragna, Mara S., Machado, Ivan C., Casimiro, Fernanda M.S., Neves, Precil D.M.M., Palma, Lilian M., Varela, Patrícia, Vaisbich, Maria H., Marie, Suely K.N., Facincani, Inalda, Pesquero, João B., Belangero, Vera M.S., Sampson, Matthew G., Koch Nogueira, Paulo C., Onuchic, Luiz F.
Publicado 2019