These authors contributed equally to this work.
Amplicon-based high-throughput pooled sequencing identifies mutations in CYP7B1 and SPG7 in sporadic spastic paraplegia patients
Article first published online: 13 JUN 2011
© 2011 John Wiley & Sons A/S
Special Issue: Exome Sequencing
Volume 80, Issue 2, pages 148–160, August 2011
How to Cite
Schlipf, N., Schüle, R., Klimpe, S., Karle, K., Synofzik, M., Schicks, J., Riess, O., Schöls, L. and Bauer, P. (2011), Amplicon-based high-throughput pooled sequencing identifies mutations in CYP7B1 and SPG7 in sporadic spastic paraplegia patients. Clinical Genetics, 80: 148–160. doi: 10.1111/j.1399-0004.2011.01715.x
- Issue published online: 12 JUL 2011
- Article first published online: 13 JUN 2011
- Accepted manuscript online: 27 MAY 2011 09:49AM EST
- Received 10 May 2011, revised and accepted for publication 24 May 2011
The following Supporting information is available for this article:
Table S1. Primers for all coding exons and intron boundaries of the CYP7B1 gene and SPG7 gene.
Table S2. Lib-L adaptor–barcode–primer.
Table S3. Lib-A adaptor–barcode–primer.
Additional Supporting information may be found in the online version of this article.
|CGE_1715_sm_ts1-ts3.doc||178K||Supporting info item|
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