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- W2895923275 abstract "Due to its frequency and the implications of early detection, hearing impairment has become an important epidemiological and public health care problem. Del35G/GJB2 mutation is the most common cause of genetic deafness, visualized by the PCR method. The mutation analysis has been successfully introduced in the diagnostics of deafness, and it enables fast, precise and etiologic diagnosis, as well as informative genetic counselling. The study of the Croatian population from the counties of Istria and Primorje-Gorski kotar revealed that the del35G mutation is involved in 36% of hearing impaired subjects; the incidence of the mutation in the population of newborns being 1/1091 (95CI: 1/372 – 1/3205)." @default.
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- W2895923275 date "2004-01-01" @default.
- W2895923275 modified "2023-09-28" @default.
- W2895923275 title "MUTACIJE U GENU GJB2/CONNEXIN 26 KAO NAJČEŠĆI UZROK OSLABLJENOG SLUHA" @default.
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