Associated Papers
Seven Novel and Three Known Mutations in FOXL2 in 10 Chinese Families with Blepharophimosis Syndrome.
Lin B et al.
Current Molecular Medicine, 2018
A novel FOXL2 mutation in a Chinese family with blepharophimosis, ptosis, epicanthus inversus syndrome.
Tan H et al.
Human Genome Variation, 2015
[Deletion and mutation analysis to FOXL2 in blepharophimosis-ptosis-epicanthus inversus syndrome].
Zhou ZM et al.
[zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology, 2010
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