Mild Recessive Mutations in Six Fraser Syndrome–Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract

Congenital anomalies of the kidney and urinary tract (CAKUT) account for approximately 40% of children with ESRD in the United States. Hitherto, mutations in 23 genes have been described as causing autosomal dominant isolated CAKUT in humans. However, >90% of cases of isolated CAKUT still remain...

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Bibliografski detalji
Glavni autori: Kohl, Stefan, Hwang, Daw-Yang, Dworschak, Gabriel C., Hilger, Alina C., Saisawat, Pawaree, Vivante, Asaf, Stajic, Natasa, Bogdanovic, Radovan, Reutter, Heiko M., Kehinde, Elijah O., Tasic, Velibor, Hildebrandt, Friedhelm
Format: Artigo
Jezik:Inglês
Izdano: American Society of Nephrology 2014
Teme:
Brief Communications
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4147986/
https://ncbi.nlm.nih.gov/pubmed/24700879
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2013101103
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