Article

Novel SOX2 Mutation in Autosomal Dominant Cataract-Microcornea Syndrome

2021-11-30

Abstract excerpt

<h4>Background: </h4> Congenital cataract-microcornea syndrome (CCMC) is characterized by the association of congenital cataract and microcornea without any other systemic anomaly or dysmorphism. Although several causative genes have been reported in patients with CCMC, the genetic etiology of CCMC is yet to be clearly understood. <h4>Purpose: </h4> To unravel the genetic cause of autosomal dominant family with CC...

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Literature Corpus work: 74e64236-3b1e-507c-a02d-018e5b227e56
DOI: 10.21203/rs.3.rs-1085640/v1

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