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Mutations in crystallin genes result in congenital cataract associated with other ocular abnormalities
PURPOSE: This study aims to describe the phenotypes and identify pathogenic mutations in Chinese patients who have congenital cataracts associated with other ocular abnormalities. METHODS: Eleven patients from four unrelated Chinese families plus two simplex cases were enrolled in this study. Detail...
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| Publicado no: | Mol Vis |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Molecular Vision
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5757854/ https://ncbi.nlm.nih.gov/pubmed/29386872 |
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