Y. Horikawa, N. Iwasaki, and M. Hara, Mutation in hepatocyte nuclear factor???1?? gene (TCF2) associated with MODY, Nature Genetics, vol.46, issue.4, pp.384-389, 1997.
DOI : 10.1038/ng0696-161

R. Clissold, A. Hamilton, and A. Hattersley, HNF1B-associated renal and extra-renal disease???an expanding clinical spectrum, Nature Reviews Nephrology, vol.129, issue.2, pp.102-114, 2015.
DOI : 10.1038/ncpneph0807

D. Bockenhauer and G. Jaureguiberry, HNF1B-associated clinical phenotypes: the kidney and beyond, Pediatric Nephrology, vol.86, issue.364, pp.707-721, 2016.
DOI : 10.1038/ki.2014.202

E. Edgill, C. Binghal, and S. Ellard, Mutations in hepatocyte nuclear factor-1?? and their related phenotypes, Journal of Medical Genetics, vol.43, issue.1, pp.84-90, 2006.
DOI : 10.1136/jmg.2005.032854

K. Owen and A. Hattersley, Maturity-onset diabetes of the young: from clinical description to molecular genetic characterization, Best Practice & Research Clinical Endocrinology & Metabolism, vol.15, issue.3, pp.309-332, 2001.
DOI : 10.1053/beem.2001.0148

M. Nakayama, K. Nozu, and Y. Goto, HNF1B alterations associated with congenital anomalies of the kidney and urinary tract, Pediatric Nephrology, vol.307, issue.6, pp.1073-1082, 2010.
DOI : 10.7326/0003-4819-140-7-200404060-00009

A. Raaijmakers, A. Gorveleyn, and K. Devriendt, Criteria for HNF1B analysis in patients with congenital abnormalities of kidney and urinary tract, Nephrology Dialysis Transplantation, vol.30, issue.5, pp.835-877, 2015.
DOI : 10.1093/ndt/gfu370

S. Fajans, G. Bell, and K. Polonsky, Molecular Mechanisms and Clinical Pathophysiology of Maturity-Onset Diabetes of the Young, New England Journal of Medicine, vol.345, issue.13, pp.971-80, 2001.
DOI : 10.1056/NEJMra002168