Publication | Closed Access

Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: A report of five novel mutations

Developmental BiologyMendelian DisorderGenetic DisorderGeneticsAudiologyNovel MutationsAuditory PhysiologyAuditory ResearchAuditory ScienceHuman HearingArtsMedicineAuditory SystemHearing Loss