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...

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Detalhes bibliográficos
Publicado no:Int J Biol Sci
Main Authors: Zhang, Leilei, He, Jie, Han, Bing, Lu, Linna, Fan, Jiayan, Zhang, He, Ge, Shengfang, Zhou, Yixiong, Jia, Renbing, Fan, Xianqun
Formato: Artigo
Idioma:Inglês
Publicado em: Ivyspring International Publisher 2016
Assuntos:
Research Paper
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4997055/
https://ncbi.nlm.nih.gov/pubmed/27570485
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7150/ijbs.13774
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