Targeted sequencing of 96 renal developmental microRNAs in 1213 individuals from 980 families with congenital anomalies of the kidney and urinary tract

BACKGROUND: Congenital anomalies of the kidney and urinary tract (CAKUT) are the most common cause of chronic kidney diseases in children and young adults, accounting for ∼50% of cases. These anomalies represent maldevelopment of the genitourinary system and can be genetically explained in only 10–1...

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Vydáno v:Nephrol Dial Transplant
Hlavní autoři: Kohl, Stefan, Chen, Jing, Vivante, Asaf, Hwang, Daw-Yang, Shril, Shirlee, Dworschak, Gabriel C., Van Der Ven, Amelie, Sanna-Cherchi, Simone, Bauer, Stuart B., Lee, Richard S., Soliman, Neveen A., Kehinde, Elijah O., Reutter, Heiko M., Tasic, Velibor, Hildebrandt, Friedhelm
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2016
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Original Articles
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4967727/
https://ncbi.nlm.nih.gov/pubmed/26908769
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ndt/gfv447
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