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Long-term outcome in a case series of Denys–Drash syndrome
BACKGROUND: Denys–Drash syndrome (DDS) is a rare disease caused by mutations in exons 8 and 9 of the WT1 gene. It is characterized by the association of early onset steroid-resistant nephrotic syndrome (SRNS), Wilms’ tumour and, in some patients, intersex disorders, with increasing risk of gonadobla...
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| Publicado no: | Clin Kidney J |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6885669/ https://ncbi.nlm.nih.gov/pubmed/31807296 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ckj/sfz022 |
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