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

N. D.Nanna D. Rendtorff, Mei Zhu, Toril Fagerheim, Torben L. Antal, Mary Pat Jones, Tanya M. Teslovich, Elizabeth M. Gillanders, Michael Barmada, Erik Teig, Jeffrey M. Trent, Karen H. Friderici, Dietrich A. Stephan, Lisbeth Tranebjærg

Research output: Contribution to journal › Article › peer-review

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