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Novel mutations associated with autosomal-dominant congenital cataract identified in Chinese families
As the leading cause of impaired vision, congenital cataracts, particularly autosomal dominant congenital cataract (ADCC), have been considered as a hereditary disease. The present study aimed to identify genetic defects in Chinese pedigrees with ADCC. A total of 6 Chinese families with ADCC were in...
Kaydedildi:
| Yayımlandı: | Exp Ther Med |
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| Asıl Yazarlar: | , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
D.A. Spandidos
2019
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6755416/ https://ncbi.nlm.nih.gov/pubmed/31555371 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2019.7865 |
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