跳至主要内容
搜索

全基因组关联研究确定了伴随性内斜视的易感位点,并提出了亲本效应.

目的: To identify genetic variants conferring susceptibility to esotropia.
Esotropia is the most common form of comitant strabismus, has its highest
incidence in European ancestry populations, and is believed to be inherited
as a complex trait.

关闭菜单