Authors: Bespalova, IN Van Camp, G Bom, SJH Brown, DJ Cryns, K DeWan, AT Erson, AE Flothmann, K Kunst, HPM Kurnool, P Sivakumaran, TA Cremers, CWRJ Leal, SM Burmeister, M Lesperance, MM

Citation: In. Bespalova et al., Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss, HUM MOL GEN, 10(22), 2001, pp. 2501-2508

Authors: Greene, CC McMillan, PM Barker, SE Kurnool, P Lomax, MI Burmeister, M Lesperance, MM

Citation: Cc. Greene et al., DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24, AM J HU GEN, 68(1), 2001, pp. 254-260