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Zebrafish mab21l2 mutants possess severe defects in optic cup morphogenesis, lens and cornea development
BACKGROUND: Mutations in MAB21L2 result in severe ocular defects including microphthalmia, anophthalmia, coloboma, microcornea, and cataracts. The molecular and cellular underpinnings of these defects are unknown, as is the normal cellular function of MAB21L2. Zebrafish mab21l2(au10) mutants possess...
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| 出版年: | Dev Dyn |
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| 主要な著者: | , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2019
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6602828/ https://ncbi.nlm.nih.gov/pubmed/31037784 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/dvdy.44 |
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