Concepedia

Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31

Xue-Zhong Liu, Yongyi Yuan, Denise Yan, Emilie Hong Ding, Xiao Mei Ouyang, Fei Yu, Wenxue Tang, Huijun Yuan, Qing Chang, Li Du,

Human Genetics · 2008 · 116 citations · 45 references

DOI

Concepts

References

45

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

David P. Kelsell, John Dunlop, Howard P. Stevens et al. · Nature · 1997 · 1.5K citations

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Specific permeability and selective formation of gap junction channels in connexin-transfected HeLa cells.

C. Elfgang, Reiner Eckert, Hella Lichtenberg‐Fraté et al. · The Journal of Cell Biology · 1995 · 818 citations · Full text

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Multisubunit assembly of an integral plasma membrane channel protein, gap junction connexin43, occurs after exit from the ER

Linda S. Musil, Daniel A. Goodenough · Cell · 1993 · 495 citations

, , +15

Mutations in the gene encoding gap junction protein β-3 associated with autosomal dominant hearing impairment

Jia-Hui Xia, Chunyu Liu, Bei-sha Tang et al. · Nature Genetics · 1998 · 426 citations

, , +14

Opposite voltage gating polarities of two closely related onnexins

Vytas K. Verselis, Christopher S. Ginter, Thaddeus A. Bargiello · Nature · 1994 · 360 citations

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