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Novel mutation of GJA8 in autosomal dominant congenital cataracts

BACKGROUND: Congenital cataracts is the most common cause of childhood visual impairment and blindness worldwide. It is reported that about one quarter of congenital cataracts caused by genetic defects. Various gene mutations have been identified in hereditary cataracts so far. The purpose of the pr...

詳細記述

保存先:
書誌詳細
出版年:Ann Transl Med
主要な著者: Ding, Ning, Chen, Zhengyu, Song, Xudong, Tang, Xiaoyan
フォーマット: Artigo
言語:Inglês
出版事項: AME Publishing Company 2020
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC7576067/
https://ncbi.nlm.nih.gov/pubmed/33240976
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/atm-20-4663
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