Φορτώνει......
AAV-mediated human CNGB3 restores cone function in an all-cone mouse model of CNGB3 achromatopsia
Complete congenital achromatopsia is a devastating hereditary visual disorder. Mutations in the CNGB3 gene account for more than 50% of all known cases of achromatopsia. This work investigated the efficiency of subretinal (SR) delivered AAV8 (Y447, 733F) vector containing a human PR2.1 promoter and...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | J Biomed Res |
|---|---|
| Κύριοι συγγραφείς: | , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Editorial Department of Journal of Biomedical Research
2020
|
| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7183301/ https://ncbi.nlm.nih.gov/pubmed/32305965 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7555/JBR.33.20190056 |
| Ετικέτες: |
Προσθήκη ετικέτας
Δεν υπάρχουν, Καταχωρήστε ετικέτα πρώτοι!
|