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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...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2021
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| Materias: | |
| 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 |