Authors: Kovach, MJ Lin, JP Boyadjiev, S Campbell, K Mazzeo, L Herman, K Rimer, LA Frank, W Llewellyn, B Jabs, EW Gelber, D Kimonis, VE

Citation: Mj. Kovach et al., A unique point mutation in the PMP22 gene is associated with Charcot-Marie-Tooth disease and deafness, AM J HU GEN, 64(6), 1999, pp. 1580-1593