Identification of 34 novel and 56 known FOXL2 mutations in patients with blepharophimosis syndrome

A. Beysen, S. De Jaegere, D. Amor, P. Bouchard, S. Christin-Maitre, M. Fellous, P. Touraine, A.W. Grix, R. Hennekam, F. Meire, N. Oyen, L.C. Wilson, D. Barel, J. Clayton-Smith, T. De Ravel, C. Decock, P. Delbeke, R. Ensenauer, F. Ebinger, G. Gillessen-KaesbachY. Hendriks, V. Kimonis, R. Laframboise, P. Laissue, K. Leppig, B.P. Leroy, D.T. Miller, D. Mowat, L. Neumann, A.S. Plomp, N. Van Regemorter, D. Wieczorek, R.A. Veitia, A. De Paepe, E. De Baere

Research output: Contribution to journal/periodicalArticleScientificpeer-review

Original languageEnglish
Pages (from-to)E205-E219
JournalHuman Mutation
Volume29
DOIs
Publication statusPublished - 2008

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