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[Collagen IV (alpha3-alpha4) nephropathy].

Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia - 1 Jan 2005

Torra R, Tazón B, Ars E, Ballarín J

Abstract excerpt

Recent evidence has shown that the COL4A3, COL4A4 and COL4A5 genes are involved in different renal manifestations. Mutations in these collagen type IV genes affect the glomerular basement membrane (GBM) giving rise to a nephropathy whose symptoms range from isolated hematuria to severe renal failure. This disorder has been traditionally considered to be different entities: Autosomal Dominant Alport syndrome,...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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PMID: 16050399

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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[Collagen IV (alpha3-alpha4) nephropathy].PMID 16050399Read ↗

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Three Novel Heterozygous COL4A4 Mutations Result in Three Different Collagen Type IV Kidney Disease Phenotypes.Semantic proximity Read ↗

The clinical spectrum of type IV collagen mutations.Semantic proximity Read ↗

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Spectrum of collagen type IV nephropathies: from thin basement membrane nephropathy to Alport syndrome.Semantic proximity Read ↗

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