Nefrologia pediatrica
IDENTIFICAZIONE DI GENI CANDIDATI NELLA DETERMINAZIONE DELL’IPODISPLASIA RENALE MEDIANTE SEQUENZIAMENTO ESOMICO
comunicazione
BibliografiaReferences
[4] Wühl E, van Stralen KJ, Verrina E et al. Timing and outcome of renal replacement therapy in patients with congenital malformations of the kidney and urinary tract. Clinical journal of the American Society of Nephrology : CJASN 2013 Jan;8(1):67-74 (full text)
[8] Weber S, Taylor JC, Winyard P et al. SIX2 and BMP4 mutations associate with anomalous kidney development. Journal of the American Society of Nephrology : JASN 2008 May;19(5):891-903 (full text)
[9] Lienkamp S, Ganner A, Boehlke C et al. Inversin relays Frizzled-8 signals to promote proximal pronephros development. Proceedings of the National Academy of Sciences of the United States of America 2010 Nov 23;107(47):20388-93 (full text)