| 1 | DFNB34, GJA1, GJA1P1
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| Novel mutations in the connexin43 (GJA1) and GJA1 pseudogene may contribute to nonsyndromic hearing loss.
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| Hong HM, Yang JJ, Shieh JC, Lin ML, Li SY.
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| Hum Genet 127(5):545-51. Epub 2010 Feb 4. Erratum in: Hum Genet. 2010 Mar;127(5):553. Li, Mei-Ling [corrected to Lin, Mei-Ling]. 2010
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| 2 | DFNB3, DFNB30, MYO3A, DFNB34
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| From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30.
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| Walsh T, Walsh V, Vreugde S, Hertzano R, Shahin H, Haika S, Lee MK, Kanaan M, King MC, Avraham KB.
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| Proc Natl Acad Sci U S A 99(11):7518-23. 2002
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| 3 | DFNB34, GJA1
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| Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness.
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| Liu XZ, Xia XJ, Adams J, Chen ZY, Welch KO, Tekin M, Ouyang XM, Kristiansen A, Pandya A, Balkany T, Arnos KS, Nance WE.
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| Hum Mol Genet 10(25):2945-51. 2001
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