Yüklüyor......
Genetic Testing as a New Standard for Clinical Diagnosis of Color Vision Deficiencies
PURPOSE: The genetics underlying inherited color vision deficiencies is well understood: causative mutations change the copy number or sequence of the long (L), middle (M), or short (S) wavelength sensitive cone opsin genes. This study evaluated the potential of opsin gene analyses for use in clinic...
Kaydedildi:
| Yayımlandı: | Transl Vis Sci Technol |
|---|---|
| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
The Association for Research in Vision and Ophthalmology
2016
|
| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5017313/ https://ncbi.nlm.nih.gov/pubmed/27622081 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/tvst.5.5.2 |
| Etiketler: |
Etiketle
Etiket eklenmemiş, İlk siz ekleyin!
|