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A novel FOXL2 mutation was identified in one family with both types of blepharophimosis-ptosis-epica
【机 构】
:
Department of Ophthalmology,Renmin Hospital of Wuhan University
【出 处】
:
中华医学会第十五次全国医学遗传学学术会议、中国医师协会医学遗传医师分会第一届全国学术会议暨2016年浙江省医学遗传学年会
【发表日期】
:
2016年5期
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