Associated Papers
Connexin Mutations and Hereditary Diseases.
Qiu Y et al.
International Journal of Molecular Sciences, 2022
GJB2 Gene Mutations in Syndromic Skin Diseases with Sensorineural Hearing Loss.
Iossa S et al.
Current Genomics, 2011
Three novel connexin26 gene mutations in autosomal recessive non-syndromic deafness.
Fuse Y et al.
Neuroreport, 1999
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