Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder

Vogt, J, Mussotter, T, Bengesser, K, Claes, K, Högel, J, Chuzhanova, N ORCID: 0000-0002-4655-3618, Fu, C, Van den Ende, J, Mautner, VF, Cooper, DN, 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. Human Mutation, 33 (11), pp. 1599-1609.

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Item Type: Journal article
Publication Title: Human Mutation
Creators: 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.
Date: 2012
Volume: 33
Number: 11
Divisions: Schools > School of Science and Technology
Depositing User: EPrints Services
Date Added: 09 Oct 2015 10:20
Last Modified: 09 Jun 2017 13:26
URI: http://irep.ntu.ac.uk/id/eprint/11507

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