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Novel FOXC2 Mutation in Hereditary Distichiasis Impairs DNA-Binding Activity and Transcriptional Activation
Distichiasis presents as double rows of eyelashes arising from aberrant differentiation of the meibomian glands of the eyelids, and it may be sporadic or hereditary. FOXC2 gene mutations in hereditary distichiasis are rarely reported. Here, we examined two generations of a Chinese family with heredi...
Autores principales: | Zhang, Leilei, He, Jie, Han, Bing, Lu, Linna, Fan, Jiayan, Zhang, He, Ge, Shengfang, Zhou, Yixiong, Jia, Renbing, Fan, Xianqun |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4997055/ https://www.ncbi.nlm.nih.gov/pubmed/27570485 http://dx.doi.org/10.7150/ijbs.13774 |
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