Nature Genet. 20, 370–373 (1998).
One of the two GJB3 mutations we described lies at amino acid position 183. The mutation results in the substitution of a lysine residue for a glutamate residue, rather than a glutamine residue, as we originally proposed. We thank Andrew Griffith, of the US National Institutes of Health, for bringing this to our attention.
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The online version of the original article can be found at 10.1038/3845
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Xia, Jh. Correction: Mutations in the gene encoding gap junction protein β–3 associated with autosomal dominant hearing impairment. Nat Genet 21, 241 (1999). https://doi.org/10.1038/6067
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DOI: https://doi.org/10.1038/6067
