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MicroRNAs: potential regulators of renal development genes that contribute to CAKUT
Congenital anomalies of the kidney and urinary tract (CAKUT) are the leading cause of childhood chronic kidney disease (CKD). While mutations in several renal development genes have been identified as causes for CAKUT, most cases have not yet been linked to known mutations. Furthermore, the genotype...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3944105/ https://ncbi.nlm.nih.gov/pubmed/23996519 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00467-013-2599-0 |
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