Article
FOXL2 gene mutations and blepharophimosis-ptosis-epicanthus inversus syndrome (BPES): a novel mutation detected in a Chinese family and a statistic model for summarizing previous reported records.
Mutagenesis - 1 Sept 2009
Xu Yan, Lei Huo, Dong Hong, Zhang Liping, Qin Qionglian, Gao Jianmei, Zou Yunlian, Yan Xinmin
Abstract excerpt
Previous studies found that the forkhead transcription factor 2 (FOXL2) gene mutations are responsible for both types of blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) but have not established any systematic statistic model for the complex and even contradictory results about genotype-phenotype correlations between them. This study is aimed to find possible mutations of FOXL2 gene in a Chinese family...
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