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Novel Mutations of PAX6 and WFS1 Associated With Congenital Cataract in a Chinese Family
Background: Congenital cataract is a common cause of blindness in childhood. About half of the cases have a genetic etiology, and more than 100 genes have been associated with congenital cataracts. This study reports the clinical and genetic findings of a two-generation Chinese family affected by co...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Cureus
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9957680/ https://www.ncbi.nlm.nih.gov/pubmed/36843716 http://dx.doi.org/10.7759/cureus.34208 |