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Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment.
Nat Genet. 1998 May;19(1):60-2. doi: 10.1038/ng0598-60.
Nat Genet. 1998.
PMID: 9590290
A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.
Verhoeven K, Van Camp G, Govaerts PJ, Balemans W, Schatteman I, Verstreken M, Van Laer L, Smith RJ, Brown MR, Van de Heyning PH, Somers T, Offeciers FE, Willems PJ.
Verhoeven K, et al.
Am J Hum Genet. 1997 May;60(5):1168-73.
Am J Hum Genet. 1997.
PMID: 9150164
Free PMC article.
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