Clinical and histopathological characteristics of COL4A3 c.2881+1G>A variant causing Alport spectrum disorders in Croatian population
Article in Biomolecules and Biomedicine (July 2022)
The most recent citing publications are shown below. View all 41 publications that cite this research output on Dimensions.
Hereditary and familial diseases and malformations of kidneys in childhood
Article in Child's Health (September 2021)
A novel variant in the COL4A3 gene: etiology of Alport syndrome type 2 in a 38-year-old male with suspected hereditary kidney disease
Article in Advances in Laboratory Medicine / Avances en Medicina de Laboratorio (July 2021)