Journal article
Do mutations in COL4A1 or COL4A2 cause thin basement membrane nephropathy (TBMN)?
Ke Wei Zhang, Stephen Tonna, Yan Yan Wang, Kesha Rana, Smitha Padavarat, Judy Savige
Pediatric Nephrology | Springer Science and Business Media LLC | Published : 2007
Abstract
Thin basement membrane nephropathy (TBMN) is the commonest cause of persistent glomerular haematuria and often presents in childhood. Only 40% of affected individuals have mutations identified in the COL4A3 and COL4A4 genes, but mutations in the genes for other COL4A isoforms also result in thinned membranes in humans (COL4A5) and mice (COL4A1). This study examined whether COL4A1/COL4A2 represented a further genetic locus for TBMN. Nine families with TBMN in whom haematuria did not segregate with COL4A3/COL4A4, were examined for linkage to COL4A1/COL4A2 using five micro-satellite markers. In addition, index cases from these families plus a further 14 unrelated individuals with TBMN that was ..
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