Single amino acid variation in MAB21L1 is dominantly associated with congenital eye defects.
Fanlei MengXin LiJinlu ZhangZhiyang GaoXue YangZiqi LiuYajie LiuTong GuoLikun WangLiping YangZhaohui WangPublished in: Journal of medical genetics (2022)
in the genetic testing panel for congenital eye disorders.
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