Source: Pediatric nephrology. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, NEFROPATIAS (GENÉTICA), EVOLUÇÃO CLÍNICA, PROTEINÚRIA
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SILVA, Thatiana Evilen da et al. A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46, XY patient with denys-Drash syndrome. Pediatric nephrology, v. 26, n. 8, p. 1311-1315, 2011Tradução . . Disponível em: https://doi.org/10.1007/s00467-011-1847-4. Acesso em: 09 maio 2024.APA
Silva, T. E. da, Nishi, M. Y., Costa, E. M. F., Martin, R. M., Carvalho, F. M., Mendonça, B. B., & Domenice, S. (2011). A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46, XY patient with denys-Drash syndrome. Pediatric nephrology, 26( 8), 1311-1315. doi:10.1007/s00467-011-1847-4NLM
Silva TE da, Nishi MY, Costa EMF, Martin RM, Carvalho FM, Mendonça BB, Domenice S. A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46, XY patient with denys-Drash syndrome [Internet]. Pediatric nephrology. 2011 ; 26( 8): 1311-1315.[citado 2024 maio 09 ] Available from: https://doi.org/10.1007/s00467-011-1847-4Vancouver
Silva TE da, Nishi MY, Costa EMF, Martin RM, Carvalho FM, Mendonça BB, Domenice S. A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46, XY patient with denys-Drash syndrome [Internet]. Pediatric nephrology. 2011 ; 26( 8): 1311-1315.[citado 2024 maio 09 ] Available from: https://doi.org/10.1007/s00467-011-1847-4