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SIX1gene: absence of mutations in children with isolated congenital anomalies of kidney and urinary tract

โœ Scribed by Negrisolo, Susanna; Centi, Sonia; Benetti, Elisa; Ghirardo, Giulia; Della Vella, Manuela; Murer, Luisa; Artifoni, Lina

Book ID
125392313
Publisher
Wichtig Editore
Year
2014
Tongue
English
Weight
280 KB
Volume
27
Category
Article
ISSN
1121-8428

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โœ Stefania Gimelli; Gianluca Caridi; Silvana Beri; Kyle McCracken; Renata Bocciard ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 340 KB ๐Ÿ‘ 1 views

Congenital anomalies of the kidney and the urinary tract (CAKUT) represent a major source of morbidity and mortality in children. Several factors (PAX, SOX,WNT, RET, GDFN, and others) play critical roles during the differentiation process that leads to the formation of nephron epithelia. We have ide