PBX1 haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humans
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| Description | scientific article published on 7 March 2017 |
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author: Pauline Le Tanno Radu Harbuz Florence Amblard Caroline Bosson Véronique Satre Antonio Novelli Klaus Dieterich Ida Vogel Sylvie Jaillard Pierre F Ray Marie Bidart Pierre-Simon Jouk Charles Coutton Hervé Sartelet Frederique Sloan Bena |
| Publication date | March 7, 2017 |
| Language | English |
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