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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Detalles Bibliográficos
Autores principales: Zhang, Leilei, He, Jie, Han, Bing, Lu, Linna, Fan, Jiayan, Zhang, He, Ge, Shengfang, Zhou, Yixiong, Jia, Renbing, Fan, Xianqun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2016
Materias:
Research Paper
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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