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Posterior Polymorphous Corneal Dystrophy 3 is Associated with Agenesis and Hypoplasia of the Corpus Callosum
Posterior polymorphous corneal dystrophy (PPCD) is a dominantly inherited disorder of the corneal endothelium that has been associated with mutations in the zinc-finger E-box binding homeobox 1 gene (ZEB1) gene in approximately one-third of affected families. While the corneal dystrophies have tradi...
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| Autori principali: | , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2014
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4074516/ https://ncbi.nlm.nih.gov/pubmed/24780443 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.visres.2014.04.007 |
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