Testing for the cytosine insertion in the VNTR of the MUC1 gene in a cohort of Italian patients with autosomal dominant tubulointerstitial kidney disease

Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management—A KDIGO consensus report

(2015) Kai-Uwe Eckardt et al.   KIDNEY INTERNATIONAL

Variable Clinical Presentation of an MUC1 Mutation Causing Medullary Cystic Kidney Disease Type 1

(2014) A. J. Bleyer et al.   Clinical Journal of the American Society of Nephrology

Unexpectedly high prevalence of rare genetic disorders in kidney transplant recipients with an unknown causal nephropathy

(2014) Marco Quaglia et al.   CLINICAL TRANSPLANTATION

Renal fibrosis is the common feature of autosomal dominant tubulointerstitial kidney diseases caused by mutations in mucin 1 or uromodulin

(2014) Arif B. Ekici et al.   KIDNEY INTERNATIONAL

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

(2014) Claudio Musetti et al.   NEPHROLOGY

Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing

(2013) Andrew Kirby et al.   NATURE GENETICS

Risk of de novo cancers after transplantation: Results from a cohort of 7217 kidney transplant recipients, Italy 1997–2009

(2012) Pierluca Piselli et al.   EUROPEAN JOURNAL OF CANCER

Hereditary Interstitial Kidney Disease

(2010) Anthony J. Bleyer et al.   SEMINARS IN NEPHROLOGY