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Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations
Background and objectives: The risk of developing Wilms tumor (WT) can be present or absent in patients with nephrotic syndrome (NS) caused by WT1 mutations. Here, the genotype/phenotype correlation regarding the outcome and risk for WT in 52 patients from 51 families with NS due to WT1 mutations is...
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| Main Authors: | , , , , , , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
American Society of Nephrology
2010
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2974408/ https://ncbi.nlm.nih.gov/pubmed/20595692 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2215/CJN.09351209 |
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