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Gonadal Function in 15 Patients Associated with WT1 Gene Mutations
Denys-Drash syndrome (DDS) and Frasier syndrome (FS) are caused by mutations of the WT1 gene. These disorders are characterized by renal disease, abnormality of male sex differentiation, and Wilms’ tumor and gonadoblastoma. There have been few reports on gonadal function in a large series of patient...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
The Japanese Society for Pediatric Endocrinology
2006
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4004866/ https://ncbi.nlm.nih.gov/pubmed/24790335 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1297/cpe.15.143 |
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