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Exome sequencing identifies a novel missense mutation of WFS1 as the cause of non-syndromic low-frequency hearing loss in a Chinese family

Chinese FamilyMendelian DisorderGenetic DisorderGeneticsAudiologyArtsHearing DisordersAuditory ResearchAuditory ScienceHuman HearingSystems BiologyMedicineAuditory SystemNovel Missense MutationHearing Loss