Detalhe da pesquisa
1.
Clinical Significance of the Cystic Phenotype in Alport Syndrome.
Am J Kidney Dis
; 2024 Mar 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38514012
2.
Monoallelic pathogenic IFT140 variants are a common cause of autosomal dominant polycystic kidney disease-spectrum phenotype.
Clin Kidney J
; 17(2): sfae026, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38404363