Just published in Kidney International Reports | Renal and Extrarenal Phenotypes in Patients With HNF1B Variants and Chromosome 17q12 Microdeletions

Discover groundbreaking insights into how HNF1B variants impact kidney survival in patients with chronic kidney disease.

Dear colleagues

We are pleased to announce the publication of a new study titled "Renal and Extrarenal Phenotypes in Patients With HNF1B Variants and Chromosome 17q12 Microdeletions," is now available in Kidney International Reports. This study offers significant insights into the correlation between specific HNF1B gene variants and the progression of chronic kidney disease (CKD) using data from the ERKNet registries

The International Society of Nephrology (ISN) also played a key role in supporting this work, alongside the Neocyst consortium, whose collaboration was crucial in advancing this research.

Read the full document herehttps://www.kireports.org/article/S2468-0249(24)01715-7/fulltext#articleInformation

Thank you to all who contributed to this work!

Your ERKNet Team


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