Congenital cataract: a guide to genetic and clinical management
Worldwide 20,000–40,000 children with congenital or childhood cataract are born every year with varying degrees and patterns of lens opacification with a broad aetiology. In most cases of bilateral cataract, a causative genetic mutation can be identified, with autosomal dominant inheritance being mo...
محفوظ في:
| المؤلفون الرئيسيون: | , , , |
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| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
SAGE Publishing
2020-07-01
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| سلاسل: | Therapeutic Advances in Rare Disease |
| الوصول للمادة أونلاين: | https://doi.org/10.1177/2633004020938061 |
| الوسوم: |
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