COL4A5 and LAMA5 variants co-inherited in familial hematuria: digenic inheritance or genetic modifier effect?-Reference-Cited by-同舟云学术

COL4A5 and LAMA5 variants co-inherited in familial hematuria: digenic inheritance or genetic modifier effect?

Published:2018-05-16 Issue:1 Volume:19 Page:
ISSN:1471-2369
Container-title:BMC Nephrology
language:en
Short-container-title:BMC Nephrol

Author:

Voskarides Konstantinos,Papagregoriou Gregory,Hadjipanagi Despina,Petrou Ioanelli,Savva Isavella,Elia Avraam,Athanasiou Yiannis,Pastelli Androulla,Kkolou Maria,Hadjigavriel Michalis,Stavrou Christoforos,Pierides Alkis,Deltas Constantinos

Funder

Cyprus Research Promotion Foundation

Publisher

Springer Science and Business Media LLC

Subject

Nephrology

Link

http://link.springer.com/content/pdf/10.1186/s12882-018-0906-5.pdf

Reference35 articles.

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3. Savige J, Rana K, Tonna S, Buzza M, Dagher H, Wang YY. Thin basement membrane nephropathy. Kidney Int. 2003;64(4):1169–78.

4. Gregory MC. The clinical features of thin basement membrane nephropathy. Semin Nephrol. 2005;25(3):140–5.

5. Haas M. Alport syndrome and thin glomerular basement membrane nephropathy: a practical approach to diagnosis. Arch Pathol Lab Med. 2009;133(2):224–32.

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