Phenotype and Outcome in Hereditary Tubulointerstitial Nephritis Secondary to UMOD Mutations

SUMMARY: BACKGROUND: UMOD mutations cause familial juvenile hyperuricemic nephropathy (FJHN) and medullary cystic kidney disease (MCKD), although these phenotypes are nonspecific. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: We reviewed cases of UMOD mutations diagnosed in the genetic laborato...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Bollée, Guillaume, Dahan, Karin, Flamant, Martin, Morinière, Vincent, Pawtowski, Audrey, Heidet, Laurence, Lacombe, Didier, Devuyst, Olivier, Pirson, Yves, Antignac, Corinne, Knebelmann, Bertrand
Format: Artigo
Idioma:Inglês
Publicat: American Society of Nephrology 2011
Matèries:
Original Articles
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3359549/
https://ncbi.nlm.nih.gov/pubmed/21868615
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2215/CJN.01220211
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars