Associated Papers
The pathogenesis of common Gjb2 mutations associated with human hereditary deafness in mice.
Li Q et al.
Cellular and Molecular Life Sciences : Cmls, 2023
37178259 (PubMed )
Supplement: 18_2023_4794_MOESM1_ESM.docx
The genetic bases for non-syndromic hearing loss among Chinese.
Ouyang XM et al.
Journal of Human Genetics, 2009
Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexins.
Rabionet R et al.
Human Mutation, 2000
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