Functional Consequences of Pathogenic Variants of the GJB2 Gene (Cx26) Localized in Different Cx26 Domains

Research output: Contribution to journal › Review article › peer-review

Humans, Connexin 26/genetics, Connexins/genetics, Deafness/genetics, Hearing Loss/genetics, Hearing Loss, Sensorineural/genetics, Mutation, GJB2, hereditary hearing loss, non-synonymous variants, Cx26 domains

ID: 57516377

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