Differential Apoptotic and Proliferative Activities of Wild-type FOXL2 and Blepharophimosis-ptosis-epicanthus Inversus Syndrome (BPES)-associated Mutant FOXL2 Proteins
FOXL2 is an essential transcription factor that is required for proper development of the ovary and eyelid. Mutations in FOXL2 cause an autosomal dominant genetic disorder, blepharophimosis-ptosis-epicanthus inversus syndrome (BPES). BPES type I patients have eyelid malformation and premature ovari...
| Main Authors: | , |
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| Format: | Online |
| Language: | English |
| Published: |
The Society for Reproduction and Development
2013
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3958583/ |