Comment on

• Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis.

  Richard G, Smith LE, Bailey RA, Itin P, Hohl D, Epstein EH Jr, DiGiovanna JJ, Compton JG, Bale SJ. Richard G, et al. Nat Genet. 1998 Dec;20(4):366-9. doi: 10.1038/3840. Nat Genet. 1998. PMID: 9843209
• Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment.

  Xia JH, Liu CY, Tang BS, Pan Q, Huang L, Dai HP, Zhang BR, Xie W, Hu DX, Zheng D, Shi XL, Wang DA, Xia K, Yu KP, Liao XD, Feng Y, Yang YF, Xiao JY, Xie DH, Huang JZ. Xia JH, et al. Nat Genet. 1998 Dec;20(4):370-3. doi: 10.1038/3845. Nat Genet. 1998. PMID: 9843210