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