Screening of the LTBP2 gene in 214 Chinese sporadic CYP1B1-negative patients with primary congenital glaucoma

PURPOSE: To identify deleterious mutations in the latent transforming growth factor-β–binding protein 2 (LTBP2) gene in sporadic patients with primary congenital glaucoma (PCG) from a Han Chinese population, which had been excluded for mutations in the CYP1B1 gene. METHODS: In this retrospective cas...

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Detalles Bibliográficos
Autores principales: Chen, Xueli, Chen, Yuhong, Fan, Bao Jian, Xia, Mingying, Wang, Li, Sun, Xinghuai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4885908/
https://www.ncbi.nlm.nih.gov/pubmed/27293371

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4885908/
https://www.ncbi.nlm.nih.gov/pubmed/27293371

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