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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...
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| Publicado no: | Ann Transl Med |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
AME Publishing Company
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7576067/ https://ncbi.nlm.nih.gov/pubmed/33240976 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/atm-20-4663 |
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