Both authors contributed equally to this work.
Whole Exome Sequencing Reveals Uncommon Mutations in the Recently Identified Fanconi Anemia Gene SLX4/FANCP
Version of Record online: 16 OCT 2012
© 2012 Wiley Periodicals, Inc.
Volume 34, Issue 1, pages 93–96, January 2013
How to Cite
Schuster, B., Knies, K., Stoepker, C., Velleuer, E., Friedl, R., Gottwald-Mühlhauser, B., de Winter, J. P. and Schindler, D. (2013), Whole Exome Sequencing Reveals Uncommon Mutations in the Recently Identified Fanconi Anemia Gene SLX4/FANCP. Hum. Mutat., 34: 93–96. doi: 10.1002/humu.22221
Contract grant sponsors: Schroeder-Kurth Fund at the University of Wuerzburg.
Communicated by Georgia Chenevix-Trench
- Issue online: 20 DEC 2012
- Version of Record online: 16 OCT 2012
- Accepted manuscript online: 3 OCT 2012 04:20AM EST
- Manuscript Accepted: 7 SEP 2012
- Manuscript Received: 6 JUN 2012
- Schroeder-Kurth Fund at the University of Wuerzburg
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