A truncating mutation in GPSM2 is associated with recessive non-syndromic hearing loss
Version of Record online: 15 MAR 2011
© 2011 John Wiley & Sons A/S
Volume 81, Issue 3, pages 289–293, March 2012
How to Cite
Yariz, K., Walsh, T., Akay, H., Duman, D., Akkaynak, A., King, M.-C. and Tekin, M. (2012), A truncating mutation in GPSM2 is associated with recessive non-syndromic hearing loss. Clinical Genetics, 81: 289–293. doi: 10.1111/j.1399-0004.2011.01654.x
- Issue online: 31 JAN 2012
- Version of Record online: 15 MAR 2011
- Accepted manuscript online: 23 FEB 2011 09:12AM EST
- Received 18 November 2010, revised and accepted for publication 21 February 2011
The following Supporting information is available for this article:
Fig. S1. Screening of controls for the c.1684C>T mutation.
Fig. S2. Analysis of GPSM2 cDNA in lymphoblasts.
Table S1. Primer sequences used to amplify GPSM2 exons for sequencing
Table S2. Longest autozygous regions in the studied family (genomic positions are according to Hg18)
Additional Supporting information may be found in the online version of this article.
|CGE_1654_sm_suppl.pdf||1941K||Supporting info item|
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