Associated Papers
Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden.
Adadey SM et al.
Life (basel, Switzerland), 2020
GJB4 and GJC3 variants in non-syndromic hearing impairment in Ghana.
Adadey SM et al.
Experimental Biology and Medicine (maywood, N.j.), 2020
Prospective variants screening of connexin genes in children with hearing impairment: genotype/phenotype correlation.
Yang JJ et al.
Human Genetics, 2010
A novel mutation in the connexin 29 gene may contribute to nonsyndromic hearing loss.
Hong HM et al.
Human Genetics, 2010
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