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

Nanna Dahl Rendtorff; M. Zhu; T. Fagerheim; T.L. Antal; M. Jones; T.M. Teslovich; E.M. Gillanders; M. Barmada; E. Teig; J.M. Trent; K.H. Friderici; D.A. Stephan; Lisbeth Tranebjærg

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

Nanna Dahl Rendtorff, M. Zhu, T. Fagerheim, T.L. Antal, M. Jones, T.M. Teslovich, E.M. Gillanders, M. Barmada, E. Teig, J.M. Trent, K.H. Friderici, D.A. Stephan, Lisbeth Tranebjærg

44 Citations (Scopus)

Abstract

Udgivelsesdato: 2006/10

Original language	English
Journal	European Journal of Human Genetics
Volume	14
Issue number	10
Pages (from-to)	1097-1105
Number of pages	8
ISSN	1018-4813
Publication status	Published - 2006

Cite this

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., & Tranebjærg, L. (2006). 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, 14(10), 1097-1105.

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. / Rendtorff, Nanna Dahl; Zhu, M.; Fagerheim, T. et al.

In: European Journal of Human Genetics, Vol. 14, No. 10, 2006, p. 1097-1105.

Research output: Contribution to journal › Journal article › Research › peer-review

Rendtorff, ND, Zhu, M, Fagerheim, T, Antal, TL, Jones, M, Teslovich, TM, Gillanders, EM, Barmada, M, Teig, E, Trent, JM, Friderici, KH, Stephan, DA & Tranebjærg, L 2006, '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, vol. 14, no. 10, pp. 1097-1105.

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