Identification of the forkhead transcriptional factor 2 (FOXL2) gene mutations in four Chinese families with blepharophimosis syndrome

PURPOSE: To determine the genetic origin of disease in four Chinese families with blepharophimosis syndrome. METHODS: Four Han Chinese families with blepharophimosis syndrome were ascertained and patients underwent complete physical and ophthalmic examinations. Blood samples were collected and genom...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Li, Wang, Liming, Han, Ruifang, Guan, Lifang, Fan, Baohong, Liu, Mingmei, Ying, Ming, Peng, Hao, Li, Ningdong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834601/
https://www.ncbi.nlm.nih.gov/pubmed/24265544

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834601/
https://www.ncbi.nlm.nih.gov/pubmed/24265544

Ejemplares similares