Information on the Hellenic Nephrogenetics Research Consortium is provided in the Acknowledgements.
X-linked Alport syndrome in Hellenic families: Phenotypic heterogeneity and mutations near interruptions of the collagen domain in COL4A5
Version of Record online: 13 MAR 2011
© 2011 John Wiley & Sons A/S
Volume 81, Issue 3, pages 240–248, March 2012
How to Cite
Demosthenous, P., Voskarides, K., Stylianou, K., Hadjigavriel, M., Arsali, M., Patsias, C., Georgaki, E., Zirogiannis, P., Stavrou, C., Daphnis, E., Pierides, A., Deltas, C. and the Hellenic Nephrogenetics Research Consortium (2012), X-linked Alport syndrome in Hellenic families: Phenotypic heterogeneity and mutations near interruptions of the collagen domain in COL4A5. Clinical Genetics, 81: 240–248. doi: 10.1111/j.1399-0004.2011.01647.x
- Issue online: 31 JAN 2012
- Version of Record online: 13 MAR 2011
- Accepted manuscript online: 17 FEB 2011 08:27AM EST
- Received 4 November 2010, revised and accepted for publication 14 February 2011
The following Supporting information is available for this article:
Fig. S1. Pedigrees of the six studied families where we found mutations.
Table S1. Oligonucleotide primers and conditions for PCR amplification and DNA sequencing of COL4A5 exons.
Table S2. Mutations and polymorphisms identified in COL4A5 in this work.
Additional Supporting information may be found in the online version of this article.
|CGE_1647_sm_fs1_ts1_ts2.pdf||77K||Supporting info item|
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