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Article

Three novel mutations in the COL4A5 gene in Mexican Alport syndrome patients.

Clinical genetics - 1 Sept 1999

Cruz-Robles D, García-Torres R, Antignac C, Forestier L, de la Puente S G, Correa-Rotter R, Garcia-López E, Orozco L

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Identifiers

PMID: 10563487
DOI: 10.1034/j.1399-0004.1999.560312.x

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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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Three novel mutations in the COL4A5 gene in Mexican Alport syndrome patients.PMID 10563487Read ↗

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COL4A4 mutation in thin basement membrane disease previously described in Alport syndrome11See Editorial by Monnens, p. 799Semantic proximity Read ↗

[COL4A5 genotypes and clinical characteristics of children with Alport syndrome].Semantic proximity Read ↗

Autosomal recessive Alport syndrome caused by a novel COL4A4 compound heterozygous mutation: A case report.Semantic proximity Read ↗

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Mutations in type IV collagen genes and Alport phenotypes.Semantic proximity Read ↗

Five novel mutations identified in the COL4A3, COL4A4 and COL4A5 genes in 10 families with Alport syndromeSemantic proximity Read ↗

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