Renal and Extra-Renal Phenotypes in Patients with HNF1B Variants and Chromosome 17q12 Micro Deletions
Benedicte Buffin-Meyer,Juliette Richard,Vincent Guigonis,Stefanie Weber,Jens Koenig,Laurence Heidet,Nabila Moussaoui, Jeanne-Pierrette Vu,Stanislas Faguer,Audrey Casemayou, Richa Prakash,Veronique Baudouin,Julien Hogan, Demi Alexandrou,Detlef Bockenhauer,Justine Bacchetta,Bruno Ranchin,Stepanka Pruhova,Jakub Zieg,Annie Lahoche,Christine Okorn, Violetta Antal-Konya,Denis Morin,Francesca Becherucci,Sandra Habbig,Max C. Liebau,Mathilde Mauras,Tom Nijenhuis,Brigitte Llanas,Djalila Mekahli,Julia Thumfart,Burkhard Toenshoff,Laura Massella,Philippe Eckart,Sylvie Cloarec,Alejandro Cruz,Ludwig Patzer,Gwenaelle Roussey,Isabelle Vrillon,Olivier Dunand,Lucie Bessenay,Francesca Taroni,Marcin Zaniew,Ferielle Louillet,Carsten Bergmann,Franz Schaefer,Albertien M. van Eerde,Joost P. Schanstra,Stephane Decramer KIDNEY INTERNATIONAL REPORTS（2024）
Key words
chronic kidney disease,genotype-phenotype correlation,HNF1B disease,outcome
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