Llwytho...
HNF1B and PAX2 mutations are a Common Cause of Renal Hypodysplasia in the CKiD Cohort
Malformations of the kidney and lower urinary tract are the most frequent cause of end stage renal disease in children. Mutations in HNF1B and PAX2 commonly cause of syndromic urinary tract malformation. We searched for mutations in HNF1B and PAX2 in North American children with renal aplasia and hy...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
2011
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3257470/ https://ncbi.nlm.nih.gov/pubmed/21380624 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00467-011-1826-9 |
| Tagiau: |
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