APA

Rendtorff N. D., Zhu M., Fagerheim T., Antal T. L., Jones M., Teslovich T. M., Gillanders E. M., Barmada M., Teig E., Trent J. M., Friderici K. H., Stephan D. A. & Tranebjaerg L. (20061102). 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. : European journal of human genetics : EJHG.

Chicago

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, Friderici Karen H, Stephan Dietrich A and Tranebjaerg Lisbeth. 20061102. 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. : European journal of human genetics : EJHG.

Harvard

Rendtorff N. D., Zhu M., Fagerheim T., Antal T. L., Jones M., Teslovich T. M., Gillanders E. M., Barmada M., Teig E., Trent J. M., Friderici K. H., Stephan D. A. and Tranebjaerg L. (20061102). 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. : European journal of human genetics : EJHG.

MLA

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, Friderici Karen H, Stephan Dietrich A and Tranebjaerg Lisbeth. 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. : European journal of human genetics : EJHG. 20061102.