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Novel mutation of GJA8 in autosomal dominant congenital cataracts
BACKGROUND: Congenital cataracts is the most common cause of childhood visual impairment and blindness worldwide. It is reported that about one quarter of congenital cataracts caused by genetic defects. Various gene mutations have been identified in hereditary cataracts so far. The purpose of the pr...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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AME Publishing Company
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7576067/ https://www.ncbi.nlm.nih.gov/pubmed/33240976 http://dx.doi.org/10.21037/atm-20-4663 |