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Towards an understanding of kidney diseases associated with WT1 mutations
Mutations in Wilms' tumor 1 (WT1) cause a wide spectrum of renal manifestations, eventually leading to end-stage kidney failure. Insufficient understanding of WT1's molecular functions in kidney development has hampered efficient therapeutic applications for WT1-associated diseases. Recent...
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| Yayımlandı: | Kidney Int |
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| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Nature Publishing Group
2015
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4687464/ https://ncbi.nlm.nih.gov/pubmed/26154924 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ki.2015.198 |
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