Associated Papers
Next-Generation Sequencing Screening of 43 Families with Non-Syndromic Early-Onset High Myopia: A Clinical and Genetic Study.
González-Iglesias E et al.
International Journal of Molecular Sciences, 2022
Identification of a novel C-terminal extension mutation in EPHA2 in a family affected with congenital cataract.
Reis LM et al.
Molecular Vision, 2014
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