A novel WT1 heterozygous nonsense mutation (p. K248X) causing a mild and slightly progressive nephropathy in a 46‚ XY patient with Denys-Drash syndrome

da Silva‚ T.E.; Nishi‚ M.Y.; Costa‚ E.M.F.; Martin‚ R.M.; Carvalho‚ F.M.; Mendonca‚ B.B.; Domenice‚ S.

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(Reference retrieved automatically from Google Scholar through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

A novel WT1 heterozygous nonsense mutation (p. K248X) causing a mild and slightly progressive nephropathy in a 46‚ XY patient with Denys-Drash syndrome

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Author(s):	da Silva‚ T.E. ; Nishi‚ M.Y. ; Costa‚ E.M.F. ; Martin‚ R.M. ; Carvalho‚ F.M. ; Mendonca‚ B.B. ; Domenice‚ S. Total Authors: 7
Document type:	Journal article
Source:	Pediatric Nephrology; p. 1-5, 2011.

FAPESP's process:	09/03872-3 - Search of mutations in DMRT1 gene in 46,XY and 46,XX dsd (disorder of sexual development) patients due to gonadal abnormalities.
Grantee:	Thatiana Evilen da Silva
Support Opportunities:	Scholarships in Brazil - Master

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