Communicated by Claude Férec
Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder†
Version of Record online: 20 AUG 2012
© 2012 Wiley Periodicals, Inc.
Volume 33, Issue 11, pages 1599–1609, November 2012
How to Cite
Vogt, J., Mussotter, T., Bengesser, K., Claes, K., Högel, J., Chuzhanova, N., Fu, C., van den Ende, J., Mautner, V.-F., Cooper, D. N., Messiaen, L. and Kehrer-Sawatzki, H. (2012), Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder. Hum. Mutat., 33: 1599–1609. doi: 10.1002/humu.22171
- Issue online: 11 OCT 2012
- Version of Record online: 20 AUG 2012
- Accepted manuscript online: 26 JUL 2012 02:32PM EST
- Manuscript Accepted: 11 JUL 2012
- Manuscript Received: 18 APR 2012
- DFG. Grant Number: KE 724/7-1, KE 724/9-1, and KE 724/10-1
- Deutsche Krebshilfe. Grant Number: 108793 to H.K.S.
- Graduate School in Molecular Medicine, Ulm (to J.V.)
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