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Title
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.
Authors
Rendtorff ND; Zhu M; Fagerheim T; Antal TL; Jones M; Teslovich TM; Gillanders EM; Barmada M; Teig E; Trent JM; Friderici KH; Stephan DA; Tranebjaerg L
Publication
European journal of human genetics : EJHG, 2006, Vol 14, Issue 10, p1097