A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26)

Por van Wijk, E, Krieger, E, Kemperman, M, De Leenheer, E M R, Huygen, P, Cremers, C, Cremers, F, Kremer, H
Publicado em 2003

A fifth locus for otosclerosis, OTSC5, maps to chromosome 3q22–24

Por Van Den Bogaert, K, De Leenheer, E M R, Chen, W, Lee, Y, Nurnberg, P, Pennings, R, Vanderstraeten, K, Thys, M, Cremers, C, Smith, R, Van Camp, G
Publicado em 2004