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Mutation spectrum of PAX6 and clinical findings in 95 Chinese patients with aniridia
PURPOSE: Aniridia is a rare congenital panocular disease caused by mutations in PAX6. The purposes of this study were to clarify the mutation features of PAX6 in a cohort of Chinese patients with aniridia and to describe their clinical characteristics. METHODS: We recruited 95 patients from 65 unrel...
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| Udgivet i: | Mol Vis |
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| Main Authors: | , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Molecular Vision
2020
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7093334/ https://ncbi.nlm.nih.gov/pubmed/32214788 |
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