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GJA8 missense mutation disrupts hemichannels and induces cell apoptosis in human lens epithelial cells
Autosomal dominant congenital cataract (ADCC), the most common hereditary disease, is a major cause of eye disease in children. Due to its high genetic and clinical heterogeneity, the identification of ADCC-associated gene mutations is essential for the development of molecular therapies. In this st...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Nature Publishing Group UK
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6915756/ https://www.ncbi.nlm.nih.gov/pubmed/31844091 http://dx.doi.org/10.1038/s41598-019-55549-1 |