F-Actin Dysplasia Involved in Organ of Corti Deformity in Gjb2 Knockdown Mouse Model
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DOI: 10.3389/fnmol.2021.808553
Abstract: Mutations in the GJB2 gene encoding connexin26 (Cx26) protein are one of the most common causes of hereditary deafness. Previous studies have found that different Cx26-null mouse models have severe hearing loss and deformity of… read more here.
Keywords: knockdown mouse; mouse; actin; group ... See more keywords