A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46, XY patient with denys-Drash syndrome
Thatiana Evilen da Silva Mirian Yumie Nishi; Elaine Maria Frade Costa; Regina Matsunaga Martin; Filomena Marino Carvalho; Berenice Bilharinho Mendonça; Sorahia Domenice
Pediatric nephrology Berlin v. 26, n. 8, p. 1311-1315, 2011Berlin 2011
Localização: FM - Fac. Medicina (BCSEP 073 2011 )(Acessar)