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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...
Enregistré dans:
| Publié dans: | Ann Transl Med |
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| Auteurs principaux: | , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
AME Publishing Company
2020
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| Sujets: | |
| Accès en ligne: | 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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