Detection of mutations in COL4A5 in patients with Alport Syndrome

Plant, K. E., Green, P. M., Vetrie, D. and Flinter, F. A. (1999) Detection of mutations in COL4A5 in patients with Alport Syndrome. Human Mutation, 13(2), pp. 124-132. (doi:10.1002/(SICI)1098-1004(1999)13:2<124::AID-HUMU4>3.0.CO;2-Z) (PMID:10094548)

Full text not currently available from Enlighten.

Abstract

Alport syndrome (AS) can be caused by mutations in COL4A5, one of the six type IV collagen genes. For the purposes of confirming diagnoses, carrier screening and correlating genotype to phenotype, we have screened all 51 exons of this gene by SSCP analysis in 153 families with suspected AS. Mutations were identified in 77 families (of which 20 have previously been reported) and are reported with all available clinical information. All types of mutation were found (missense, nonsense, splicing, small and large deletions and insertions), with the commonest type being those affecting glycine residues in the collagen triple helix. Our 50% detection rate is similar to that of other groups and may imply the presence of mutations outside of the COL4A5 coding region or the existence of a second X-linked AS gene.

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Vetrie, Dr David
Authors: Plant, K. E., Green, P. M., Vetrie, D., and Flinter, F. A.
College/School:College of Medical Veterinary and Life Sciences > Institute of Cancer Sciences
Journal Name:Human Mutation
Publisher:Wiley
ISSN:1059-7794
ISSN (Online):1098-1004

University Staff: Request a correction | Enlighten Editors: Update this record