Article
Clinical features of hearing loss caused by STRC gene deletions/mutations in Russian population.
International journal of pediatric otorhinolaryngology - 1 Nov 2020
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
Abstract excerpt
Congenital sensorineural hearing loss is related to mutations in numerous genes encoding the structures of the inner ear in majority of the cases. Mutations in GJB2 gene are the most frequently identified causes of congenital nonsyndromal hearing loss. GJB2 gene testing became a routine clinical tool. For GJB2-negative patients new genetic approaches including methods based on new generation sequencing give a...
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