Screening and Functional Analysis of TEK Mutations in Chinese Children With Primary Congenital Glaucoma

Purposes: Recent studies have suggested that loss-of-function mutations of the tunica intima endothelial receptor tyrosine kinase (TEK) are responsible for approximately 5% of primary congenital glaucoma (PCG) cases in diverse populations. However, the causative role of TEK mutations has not been st...

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Detalles Bibliográficos
Autores principales: Qiao, Yunsheng, Chen, Yuhong, Tan, Chen, Sun, Xinghuai, Chen, Xueli, Chen, Junyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8703195/
https://www.ncbi.nlm.nih.gov/pubmed/34956319
http://dx.doi.org/10.3389/fgene.2021.764509

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8703195/
https://www.ncbi.nlm.nih.gov/pubmed/34956319
http://dx.doi.org/10.3389/fgene.2021.764509

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