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...

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Detalhes bibliográficos
Publicado no:Mol Med Rep
Main Authors: Wu, Zehua, Meng, Delong, Fang, Chengbo, Li, Jian, Zheng, Xiujie, Lin, Jiansuo, Zeng, Haijiang, Lv, Sihan, Zhang, Zhenning, Luan, Bing, Zhong, Zilin, Chen, Jianjun
Formato: Artigo
Idioma:Inglês
Publicado em: D.A. Spandidos 2019
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Articles
Acesso em linha: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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