Karin Moret

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and T-MARE regulatory sequences of HNF1β was evidenced. In conclusion, although mutations in RARE and T-MARE regulatory sequences of HNF1β may nevertheless be implicated in some renal congenital disorders, we show here that mutations in these sequences are not a frequent cause of CAKUT. More experiments are required to assess the role of the RA-MAFB-HNF1β(More)
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