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• W2106091175 abstract "Abstract. Mutations in either the COL4A3 or the COL4A4 genes, encoding the α3 and α4 chains of type IV collagen, are responsible for the autosomal-recessive form of Alport syndrome, a progressive hematuric nephropathy characterized by glomerular basement membrane abnormalities. Reported here are the complete COL4A3 exon-intron structure and a comprehensive screen for mutations of the 52 COL4A3 exons in 41 unrelated patients diagnosed as having autosomal Alport syndrome. This resulted in the identification of 21 mutations that are expected to be causative. Furthermore, it is shown that heterozygous COL4A3 missense mutations, when symptomatic, can be associated with a broad range of phenotypes, from familial benign hematuria to the complete features of Alport syndrome nephropathy." @default.
• W2106091175 created "2016-06-24" @default.
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• W2106091175 date "2001-01-01" @default.
• W2106091175 modified "2023-09-25" @default.
• W2106091175 title "Structure of the Human Type IV Collagen Gene COL4A3 and Mutations in Autosomal Alport Syndrome" @default.
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• W2106091175 doi "https://doi.org/10.1681/asn.v12197" @default.
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