The author replies
- PMID: 25826549
- PMCID: PMC4654678
- DOI: 10.1038/ki.2015.39
The author replies
Comment on
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Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis.Kidney Int. 2014 Dec;86(6):1253-9. doi: 10.1038/ki.2014.305. Epub 2014 Sep 17. Kidney Int. 2014. PMID: 25229338 Free PMC article.
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COL4A3/COL4A4 heterozygous mutations with TBMN presenting as focal segmental glomerulosclerosis.Kidney Int. 2015 Apr;87(4):859. doi: 10.1038/ki.2015.38. Kidney Int. 2015. PMID: 25826548 No abstract available.
References
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- Deltas C, Pierides A. COL4A3/COL4A4 heterozygous mutations with TBMN presenting as focal segmental glomerulosclerosis. Kidney Int. 2015 - PubMed
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- Gregory MC. The clinical features of thin basement membrane nephropathy. Semin Nephrol. 2005;25:140–145. - PubMed
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- Savige J, Rana K, Tonna S, et al. Thin basement membrane nephropathy. Kidney Int. 2003;64:1169–1178. - PubMed
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- Voskarides K, Damianou L, Neocleous V, et al. COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathy. J Am Soc Nephrol. 2007;18:3004–3016. - PubMed
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