Early Development of Hyperparathyroidism Due to Loss of<i>PTH</i>Transcriptional Repression in Patients With HNF1β Mutations?
Silvia Ferrè(Radboud University Nijmegen), Tom Nijenhuis(Radboud University Nijmegen), Joost G.J. Hoenderop(Radboud University Nijmegen), Elisabeth A. M. Cornelissen(Radboud University Medical Center), Gerben A.J. van Boekel(Radboud University Nijmegen), Johan van der Vlag(Radboud University Nijmegen), René J.M. Bindels(Radboud University Nijmegen), Ramon Sonneveld(Radboud University Nijmegen), Ernie M.H.F. Bongers(Radiotherapiegroep), Jack F.M. Wetzels(Radboud University Nijmegen)
Cited by 38
Related Papers
KDIGO 2021 Clinical Practice Guideline for the Management of Glomerular Diseases
|Kidney International|2021|2.5k
Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes
|New England Journal of Medicine|2008|811
Executive summary of the KDIGO 2021 Guideline for the Management of Glomerular Diseases
|Kidney International|2021|809
A Unified Nomenclature for the Superfamily of TRP Cation Channels
|Molecular Cell|2002|679