Fig. 1From: Whole-exome sequencing identifies a novel missense variant within LOXHD1 causing rare hearing loss in a Chinese familyPedigree, audiological evaluation and Sanger sequencing validation. a. Pedigree of this Chinese family under consanguineous marriage. The proband was indicated by arrows. “+” indicates wild type. b. Pure-tone audiometry evaluation of this proband. c. LOXHD1: c.5948C > T variants were validated by Sanger sequencingBack to article page