Autor:	Nicolina Stefania, Carucci, Gianluca, Caridi, Francesca, Lugani, Claudia, Barone, Giovanni, Conti
Rok vydání:	2019
Předmět:	Male Heterozygote Uromodulin Mutation Missense Humans Kidney Failure Chronic Child
Zdroj:	Clinical nephrology. 92(3)
ISSN:	0301-0430
Popis:	Autosomal dominant tubulointerstitial kidney disease (ADTKD) belongs to a group of renal hereditary disorders linked by common findings of tubulointerstitial disease and dominant inheritance. The renal clinical phenotype is characterized by chronic kidney disease, hyperuricemia, gout, and, inconstantly, renal cysts. Uromodulin (
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=pmid________::9ac8826a4be9f278e21b9747121d7a05 https://pubmed.ncbi.nlm.nih.gov/29424336 Zobrazit plný text záznamu