Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice

Lisenka ELM Vissers, Timothy C Cox, A Murat Maga, Kieran M Short, Fenny Wiradjaja, Irene M Janssen, Fernanda Jehee, Debora Bertola, Jia Liu, Garima Yagnik, Kiyotoshi Sekiguchi, Daiji Kiyozumi, Hans von Bokhoven, Carlo Marcelis, Michael L Cunningham, Peter J Anderson, Simeon A Boyadjiev, Maria R Passos-Bueno, Joris A Veltman, Ian M SmythMichael Buckley, Tony Roscioli

Research output: Contribution to journalArticleResearchpeer-review

49 Citations (Scopus)
Original languageEnglish
Pages (from-to)1 - 11
Number of pages11
JournalPLoS Genetics
Volume7
Issue number9 (Art. No: e1002278)
DOIs
Publication statusPublished - 2011

Cite this

Vissers, L. ELM., Cox, T. C., Maga, A. M., Short, K. M., Wiradjaja, F., Janssen, I. M., Jehee, F., Bertola, D., Liu, J., Yagnik, G., Sekiguchi, K., Kiyozumi, D., von Bokhoven, H., Marcelis, C., Cunningham, M. L., Anderson, P. J., Boyadjiev, S. A., Passos-Bueno, M. R., Veltman, J. A., ... Roscioli, T. (2011). Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice. PLoS Genetics, 7(9 (Art. No: e1002278)), 1 - 11. https://doi.org/10.1371/journal.pgen.1002278