These authors contributed equally to this work.
Whole exome sequencing identifies a novel mutation in the transglutaminase 6 gene for spinocerebellar ataxia in a Chinese family
Version of Record online: 29 MAY 2012
© 2012 John Wiley & Sons A/S
Volume 83, Issue 3, pages 269–273, March 2013
How to Cite
Li, M., Pang, S., Song, Y., Kung, M., Ho, S.-L. and Sham, P.-C. (2013), Whole exome sequencing identifies a novel mutation in the transglutaminase 6 gene for spinocerebellar ataxia in a Chinese family. Clinical Genetics, 83: 269–273. doi: 10.1111/j.1399-0004.2012.01895.x
- Issue online: 18 FEB 2013
- Version of Record online: 29 MAY 2012
- Accepted manuscript online: 3 MAY 2012 11:02AM EST
- Received 20 February 2012, revised and accepted for publication 26 April 2012
Fig. S1. The predicted tertiary structures of wild-type (a) and mutant (b) TGM6.
Appendix S1. Variant filtration and prioritization analysis by KGGSeq.
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