✦ LIBER ✦
A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment
✍ Scribed by Rendtorff, Nanna D; Zhu, Mei; Fagerheim, Toril; Antal, Torben L; Jones, MaryPat; Teslovich, Tanya M; Gillanders, Elizabeth M; Barmada, Michael; Teig, Erik; Trent, Jeffrey M
- Book ID
- 110026671
- Publisher
- Nature Publishing Group
- Year
- 2006
- Tongue
- English
- Weight
- 226 KB
- Volume
- 14
- Category
- Article
- ISSN
- 1018-4813
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