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Childhood Glaucoma Genes and Phenotypes: Focus on FOXC1 mutations causing anterior segment dysgenesis and hearing loss
Childhood glaucoma is an important cause of blindness world-wide. Eleven genes are currently known to cause inherited forms of glaucoma with onset before age 20. While all the early-onset glaucoma genes cause severe disease, considerable phenotypic variability is observed among mutations carriers. I...
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| Pubblicato in: | Exp Eye Res |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7425631/ https://ncbi.nlm.nih.gov/pubmed/31836490 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.exer.2019.107893 |
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