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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...
保存先:
| 出版年: | Ann Transl Med |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
AME Publishing Company
2020
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| 主題: | |
| オンライン・アクセス: | 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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