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• W153986935 abstract "Alport syndrome is a mainly X-linked hereditary disease of basement membranes that is characterized by progressive renal failure, deafness, and ocular lesions. It is associated with mutations of the COL4A5 gene located at Xq22 and encoding the alpha5 chain of type IV collagen. We have screened 48 of the 51 exons of the COL4A5 gene by SSCP analysis and have identified 64 mutations and 10 sequence variants among 131 unrelated Alport syndrome patients. This represents a mutation-detection rate of 50%. There were no hot-spot mutations and no recurrent mutations in our population. The identified mutations were 6 nonsense mutations, 12 frameshift mutations, 17 splice-site mutations, and 29 missense mutations, 27 of the latter being glycine substitutions in the collagenous domain. Two of these occurred on the same allele in one patient and segregated with the disease in the family. We showed that some of the glycine substitutions could be associated with the lack of immunological expression of the alpha3(IV)-alpha5(IV) collagen chains in the glomerular basement membrane." @default.
• W153986935 created "2016-06-24" @default.
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• W153986935 date "1996-12-01" @default.
• W153986935 modified "2023-10-06" @default.
• W153986935 title "Spectrum of mutations in the COL4A5 collagen gene in X-linked Alport syndrome." @default.
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• W153986935 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/1914854" @default.
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