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

Diane Beysen, Sarah De Jaegere, David Amor, Philippe Bouchard, Sophie Christin-Maitre, Marc Fellous, Philippe Touraine, Arthur W. Grix, Raoul Hennekam, Françoise Meire, Nina Oyen, Louise C. Wilson, Dalit Barel, Jill Clayton-Smith, Thomy De Ravel, Christian Decock, Patricia Delbeke, Regina Ensenauer, Friedrich Ebinger, Gabriele Gillessen-KaesbachYvonne Hendriks, Virginia Kimonis, Rachel Laframboise, Paul Laissue, Kathleen Leppig, Bart P. Leroy, David T. Miller, David Mowat, Luitgard Neumann, Astrid Plomp, Nicole Van Regemorter, Dagmar Wieczorek, Reiner A. Veitia, Anne De Paepe, Elfride De Baere

    Research output: Contribution to journal › Article › peer-review

    Fingerprint

    Dive into the research topics of 'Identification of 34 novel and 56 known FOXL2 mutations in patients with blepharophimosis syndrome'. Together they form a unique fingerprint.

    Biochemistry, Genetics and Molecular Biology