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Autosomal Recessive Nonsyndromic Neurosensory Deafness at DFNB1 Not Associated with the Compound-Heterozygous GJB2 (Connexin 26) Genotype M34T/167delT

Andrew J. Griffith, Aqeel A. Chowdhry, Kiyoto Kurima, Linda J. Hood, Bronya J.B. Keats, Charles I. Berlín, Robert J. Morell, Thomas B. Friedman

The American Journal of Human Genetics · 2000 · 69 citations · 15 references

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References

15

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

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

, , +13

Connexin-26 mutations in sporadic and inherited sensorineural deafness

Xavier Estivill, Paolo Fortina, Saul Surrey et al. · The Lancet · 1998 · 643 citations · Full text

, , +12

Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene

Françoise Denoyelle, Dominique Weil, Marion A. Maw et al. · Human Molecular Genetics · 1997 · 636 citations · Full text

, , +11

Connexin26 mutations associated with the most common form of non- syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans

Leopoldo Zelante · Human Molecular Genetics · 1997 · 627 citations

, , +16

Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis

Toshihiko Kikuchi, R. S. Kimura, DavidL. Paul et al. · Anatomy and Embryology · 1995 · 594 citations

, , +16