Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis

Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis

10.1136/jmedgenet-2012-101325

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Main Authors:	Soler, V.J., Tran-Viet, K.-N., Galiacy, S.D., Limviphuvadh, V., Klemm, T.P., St Germain, E., Fournié, P.R., Guillaud, C., Maurer-Stroh, S., Hawthorne, F., Suarez, C., Kantelip, B., Afshari, N.A., Creveaux, I., Luo, X., Meng, W., Calvas, P., Cassagne, M., Arné, J.-L., Rozen, S.G., Malecaze, F., Young, T.L.
其他作者:	DUKE-NUS GRADUATE MEDICAL SCHOOL S'PORE
格式:	Article
出版:	2014
在線閱讀:	http://scholarbank.nus.edu.sg/handle/10635/110658
標簽:	添加標簽沒有標簽, 成為第一個標記此記錄!

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