Clinical features of hearing loss caused by STRC gene deletions/mutations in Russian population

Autor: Markova, T.G., Alekseeva, N.N., Mironovich, O.L., Galeeva, N.M., Lalayants, M.R., Bliznetz, E.A., Chibisova, S.S., Polyakov, A.V., Tavartkiladze, G.A.
Zdroj: In International Journal of Pediatric Otorhinolaryngology November 2020 138
Databáze: ScienceDirect