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European Journal of Human Genetics : EJHG|June 15, 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 impairmentNanna D Rendtorff, Mei Zhu, Toril Fagerheim, et al.
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Showing results (21-30 of 21) with videos related to

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European Journal of Human Genetics : EJHG|June 15, 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 impairmentNanna D Rendtorff, Mei Zhu, Toril Fagerheim, et al.
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