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FOXE3 plays a significant role in autosomal recessive microphthalmia
FOXE3 forkhead transcription factor is essential to lens development in vertebrates. The eyes of Foxe3/foxe3-deficient mice and zebrafish fail to develop normally. In humans, autosomal dominant and recessive mutations in FOXE3 have been associated with variable phenotypes including anterior segment...
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| Hlavní autoři: | , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2010
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2998041/ https://ncbi.nlm.nih.gov/pubmed/20140963 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.33257 |
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