Genetic testing for cone rod dystrophies
We studied the scientific literature and disease guidelines in order to summarize the clinical utility of the genetic test for cone rod dystrophies (CORDs). CORDs are caused by variations in the ABCA4, ADAM9, AIPL1, C8orf37, CACNA1F, CACNA2D4, CDHR1, CNGA3, CRX, DRAM2, GUCA1A, GUCY2D, HRG4, KCNV2, P...
Kaydedildi:
| Asıl Yazarlar: | , , , , , |
|---|---|
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Sciendo
2017-10-01
|
| Seri Bilgileri: | The EuroBiotech Journal |
| Online Erişim: | https://doi.org/10.24190/ISSN2564-615X/2017/S1.11 |
| Etiketler: |
Etiket eklenmemiş, İlk siz ekleyin!
|