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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423573/
https://www.ncbi.nlm.nih.gov/pubmed/30816539
http://dx.doi.org/10.3892/mmr.2019.9989

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423573/
https://www.ncbi.nlm.nih.gov/pubmed/30816539
http://dx.doi.org/10.3892/mmr.2019.9989

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