Chronic renal failure of unknown origin is caused byHNF1Bmutations in 9% of adult patients: A single centre cohort analysis

HNF1Bdeletions in patients with young-onset diabetes but no known renal disease

(2012) E. L. Edghill et al.   DIABETIC MEDICINE

Diagnosis, management, and prognosis of HNF1B nephropathy in adulthood

(2011) Stanislas Faguer et al.   KIDNEY INTERNATIONAL

HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort

(2011) Rosemary Thomas et al.   PEDIATRIC NEPHROLOGY

Spectrum of HNF1B Mutations in a Large Cohort of Patients Who Harbor Renal Diseases

(2010) L. Heidet et al.   Clinical Journal of the American Society of Nephrology

HNF1B alterations associated with congenital anomalies of the kidney and urinary tract

(2010) Makiko Nakayama et al.   PEDIATRIC NEPHROLOGY

Expanded Clinical Spectrum in Hepatocyte Nuclear Factor 1B-Maturity-Onset Diabetes of the Young

(2009) Klemens Raile et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

HNF1B Mutations Associate with Hypomagnesemia and Renal Magnesium Wasting

(2009) S. Adalat et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Messenger RNA regulation: to translate or to degrade

(2008) Ann-Bin Shyu et al.   EMBO JOURNAL

A genetic syndrome of chronic renal failure with multiple renal cysts and early onset diabetes

(2008) Christie P. Thomas et al.   KIDNEY INTERNATIONAL