Origin of the prevalent SFTPB indel g.1549C>GAA (121ins2) mutation causing surfactant proteinB (SPB) deficiency

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Tredano, M., Cooper, D.N., Stuhrmann, M., Christodoulou, J., Chuzhanova, N.A. ORCID: 0000-0002-4655-3618, Roudot-Thoraval, F., Boëlle, P., Elion, J., Jeanpierre, M., Feingold, J., Rémy, C. and Bahuau, M., 2006. Origin of the prevalent SFTPB indel g.1549C>GAA (121ins2) mutation causing surfactant proteinB (SPB) deficiency. American Journal of Medical Genetics - A, 140, pp. 62-69.

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Item Type:	Journal article
Publication Title:	American Journal of Medical Genetics - A
Creators:	Tredano, M., Cooper, D.N., Stuhrmann, M., Christodoulou, J., Chuzhanova, N.A., Roudot-Thoraval, F., Boëlle, P., Elion, J., Jeanpierre, M., Feingold, J., Rémy, C. and Bahuau, M.
Date:	2006
Volume:	140
Divisions:	Schools > School of Science and Technology
Record created by:	EPrints Services
Date Added:	09 Oct 2015 10:05
Last Modified:	09 Jun 2017 13:18
URI:	https://irep.ntu.ac.uk/id/eprint/7446