Código QR (código de barras bidimensional)

Case Report: Wide spectrum of SALL1 variants—a rare cause of pediatric chronic kidney disease

IntroductionGenetic causes of chronic kidney disease present a diverse group. Some of them are associated with extrarenal malformations, especially ear anomalies. Genetic diagnosis is essential to confirm the diagnosis, search for additional potential manifestations, and predict the prognosis.Case p...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Principais autores: Martina Filipič, Špela Stangler Herodež, Mirjam Močnik, Sonja Golob Jančič, Nataša Marčun Varda, Danijela Krgović
Format: Artigo
Sprog:Inglês
Udgivet: Frontiers Media S.A. 2025-09-01
Serier:Frontiers in Pediatrics
Fag:
Online adgang:https://www.frontiersin.org/articles/10.3389/fped.2025.1649707/full
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!