Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis
Background Corneal intraepithelial dyskeratosis is an extremely rare condition. The classical form, affecting Native American Haliwa-Saponi tribe members, is called hereditary benign intraepithelial dyskeratosis (HBID). Herein, we present a new form of corneal intraepithelial dyskeratosis for which...
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Main Authors: | Maurer-Stroh, Sebastian, Soler, V. J., Tran-Viet, K.-N., Galiacy, S. D., Limviphuvadh, V., Klemm, T. P., St Germain, E., Fournie, P. R., Guillaud, C., Hawthorne, F., Suarez, C., Kantelip, B., Afshari, N. A., Creveaux, I., Luo, X., Meng, W., Calvas, P., Cassagne, M., Arne, J.-L., Malecaze, F., Young, T. L., Rozen, Steve G. |
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Other Authors: | School of Biological Sciences |
Format: | Article |
Language: | English |
Published: |
2013
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Subjects: | |
Online Access: | https://hdl.handle.net/10356/105013 http://hdl.handle.net/10220/16570 |
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Institution: | Nanyang Technological University |
Language: | English |
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