Prevalence of the c.35delG and p.W24X mutations in the GJB2 gene in patients with nonsyndromic hearing loss from North-West Romania

Autor: Lazăr, C., Popp, R., Trifa, A., Mocanu, C., Mihut, G., Al-Khzouz, C., Tomescu, E., Figan, I., Grigorescu-Sido, P.
Zdroj: In International Journal of Pediatric Otorhinolaryngology 2010 74(4):351-355
Databáze: ScienceDirect