Identification of a novel FOXL2 mutation in a single family...

Molecular Medicine Reports 2017 / 10 Vol. 16; Iss. 4

Identification of a novel FOXL2 mutation in a single family with both types of blepharophimosis- ptosis- epicanthus inversus syndrome

Yang, Lin, Li, Tuo, Xing, Yiqiao
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Volume:
16
Language:
english
Journal:
Molecular Medicine Reports
DOI:
10.3892/mmr.2017.7226
Date:
October, 2017
File:
PDF, 1.05 MB
english, 2017
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