Publication | Open Access

Deletions Involving Long-Range Conserved Nongenic Sequences Upstream and Downstream of FOXL2 as a Novel Disease-Causing Mechanism in Blepharophimosis Syndrome

Blepharophimosis SyndromeAutoimmune DiseaseNovel Disease-causing MechanismDisease MechanismGenetic DisorderGeneticsPathogenesisAutophagyPathologyMolecular GeneticsDisease Gene IdentificationMedicine