| 1 | DFNB30, MYO3A
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| Diagnostic application of targeted resequencing for familial nonsyndromic hearing loss.
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| Choi BY, Park G, Gim J, Kim AR, Kim BJ, Kim HS, Park JH, Park T, Oh SH, Han KH, Park WY.
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| PLoS One 8(8):e68692. doi: 10.1371/journal.pone.0068692. eCollection 2013.
2013
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| 2 | DFNB30, MYO3A
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| A mouse model for human hearing loss DFNB30 due to loss of function of myosin IIIA.
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| Walsh VL, Raviv D, Dror AA, Shahin H, Walsh T, Kanaan MN, Avraham KB, King MC.
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| Mamm Genome 22(3-4):170-7. doi: 10.1007/s00335-010-9310-6. Epub 2010 Dec 17.
2011
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| 3 | DFNB11, DFNB30, DFNB32, DFNB43, MYO3A
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| Non-syndromic, autosomal-recessive deafness.
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| Petersen MB, Willems PJ.
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| Clin Genet 69(5):371-92. Review. 2006
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| 4 | 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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