
Clinical and histopathological characteristics of COL4A3 c.2881+1G>A variant causing Alport spectrum disorders in Croatian population
Author(s) -
Matija Horaček,
Tamara Nikuševa Martić,
Petar Šenjug,
Marija Perica,
Maja Oroz,
Sania Kuzmac,
Dragan Klarić,
Merica Glavina Durdov,
Marijan Saraga,
Danko Milošević,
Danica Batinić,
Marijana Ćorić,
Frane Paić,
Danica Galešić Ljubanović
Publication year - 2022
Publication title -
bosnian journal of basic medical sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.738
H-Index - 25
eISSN - 1840-4812
pISSN - 1512-8601
DOI - 10.17305/bjbms.2022.7567
Subject(s) - medicine , focal segmental glomerulosclerosis , alport syndrome , transplantation , population , kidney disease , proteinuria , kidney transplantation , renal biopsy , membranous nephropathy , glomerulonephritis , nephropathy , pathology , gastroenterology , biopsy , kidney , diabetes mellitus , endocrinology , environmental health