Communicated by Claude Férec
Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder†
Article first published 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 published online: 11 OCT 2012
- Article first published 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.)
Additional Supporting information may be found in the online version of this article
Please note: Wiley Blackwell is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.