A novel third type of recurrent NF1 microdeletion mediated by non-allelic homologous recombination between LRRC37B-containing low-copy repeats in 17q11.2

Bengesser, K., Cooper, D.N., Steinmann, K., Kluwe, L., Chuzhanova, N.A. ORCID: 0000-0002-4655-3618, Wimmer, K., Tinschert, S., Mautner, V. and Kehrer-Sawatzki, H., 2010. A novel third type of recurrent NF1 microdeletion mediated by non-allelic homologous recombination between LRRC37B-containing low-copy repeats in 17q11.2. Human Mutation, 31, pp. 742-751.

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Item Type:	Journal article
Publication Title:	Human Mutation
Creators:	Bengesser, K., Cooper, D.N., Steinmann, K., Kluwe, L., Chuzhanova, N.A., Wimmer, K., Tinschert, S., Mautner, V. and Kehrer-Sawatzki, H.
Date:	2010
Volume:	31
Divisions:	Schools > School of Science and Technology
Record created by:	EPrints Services
Date Added:	09 Oct 2015 10:22
Last Modified:	09 Jun 2017 13:27
URI:	https://irep.ntu.ac.uk/id/eprint/11817

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