Mutations in Cx26 gene are found in most cases of human genetic deafness. Some
mutations produce syndromic deafness associated with skin disorders, like the Keratitis …

Mutations in Cx26 gene are found in most cases of human genetic deafness. Some
mutations produce syndromic deafness associated with skin disorders, like the Keratitis …

Mutations in Cx26 gene are found in most cases of human genetic deafness. Some
mutations produce syndromic deafness associated with skin disorders, like the Keratitis …

Mutations in Cx26 gene are found in most cases of human genetic deafness. Some
mutations produce syndromic deafness associated with skin disorders, like Keratitis …

Mutations in Cx26 gene are found in most cases of human genetic deafness. Some
mutations produce syndromic deafness associated with skin disorders, like the Keratitis …

Gap junction channels (GJCs) allow metabolic and electrical coupling between adjacent
cells and are formed by the oligomerization of connexin (Cx) protein subunits. Cxs …

Keratitis-Ichthyosis-Deafness Syndrome-Associated Cx26 Mutants Produce Nonfunctional Gap
Junctions but Hyperactive Hemichannels When Co-Expressed With Wild Type Cx43 | CiNii …

Mutations in Cx26 gene are found in most cases of human genetic deafness. Some
mutations produce syndromic deafness associated with skin disorders, like the Keratitis …

Mutations in Cx26 gene are found in most cases of human genetic deafness. Some
mutations produce syndromic deafness associated with skin disorders, like the Keratitis …

Gap junction channels (GJCs) allow metabolic and electrical coupling between adjacent
cells and are formed by the oligomerization of connexin (Cx) protein subunits. Cxs …