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PITX3 mutations associated with autosomal dominant congenital cataract in the Chinese population

The present study aimed to identify the disease-causing gene of a four-generation Chinese family affected with congenital posterior subcapsular cataracts (CPSC), to additionally investigate the frequency of paired like homeodomain 3 (PITX3) mutations in Chinese patients with autosomal dominant conge...

詳細記述

保存先:
書誌詳細
出版年:Mol Med Rep
主要な著者: Wu, Zehua, Meng, Delong, Fang, Chengbo, Li, Jian, Zheng, Xiujie, Lin, Jiansuo, Zeng, Haijiang, Lv, Sihan, Zhang, Zhenning, Luan, Bing, Zhong, Zilin, Chen, Jianjun
フォーマット: Artigo
言語:Inglês
出版事項: D.A. Spandidos 2019
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC6423573/
https://ncbi.nlm.nih.gov/pubmed/30816539
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/mmr.2019.9989
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