Article
Novel mutations associated with autosomal dominant congenital cataract are identified in Chinese families
2018-07-11
Abstract excerpt
<h4>Purpose</h4> As the leading cause of the impairment of vision of children, congenital cataract is considered as a hereditary disease, especially autosomal dominant congenital cataract (ADCC). The purpose of this study is to identify the genetic defect of six Chinese families with ADCC. <h4>Subjects and Methods</h4> Six Chinese families with ADCC were recruited in the study. (103 members in total, 96 members...
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Identifiers and source
- Literature Corpus work
- 309c09be-e333-5cc9-a50b-54d0767ad34d
- DOI
- 10.1101/367516
