Browsing by Subject p.D50N
Showing results 1 to 1 of 1
| Issue Date | Title | Author(s) | Rank |
|---|---|---|---|
| 2022 | Keratitis-Ichthyosis-Deafness Syndrome with heterozygous P.D50N in the GJB2 gene in two Serbian adult patients | Kalezić, T.; Vuković, I.; Stojković, M.; Stanojlović, S.; Karanović, J.; Brajušković, G. ; Savić-Pavićević, D. | M23 |