Homozygosity for uromodulin disorders: FJHN and MCKD-type 2

Homozygosity for uromodulin disorders: FJHN and MCKD-type 2. Autosomal-dominant medullary cystic kidney disease type 2 (MCKD2) and familial juvenile hyperuricemic nephropathy (FJHN) are heritable renal diseases with autosomal-dominant transmission and shared features, including polyuria, progressive...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Kidney international 2004-08, Vol.66 (2), p.558-563
Hauptverfasser:	Rezende-Lima, Wânia, Parreira, Kleber S., García-González, Miguel, Riveira, Eva, Banet, Julio F., Lens, Xosé M.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Biological and medical sciences Female Haplotypes homozygosity Homozygote Humans Male MCKD type 2 Medical sciences Middle Aged Mucoproteins - genetics Mucoproteins - urine Mutation, Missense Nephrology. Urinary tract diseases Pedigree Phenotype Polycystic Kidney, Autosomal Dominant - genetics Severity of Illness Index Uromodulin
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!