These authors contributed equally to this work.
Amplicon-based high-throughput pooled sequencing identifies mutations in CYP7B1 and SPG7 in sporadic spastic paraplegia patients
Version of Record 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 online: 12 JUL 2011
- Version of Record 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
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