Publication | Closed Access
A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.
22
Citations
32
References
2015
Year
Novel MutationMendelian DisorderMoroccan FamilyGenetic DisorderGeneticsAudiologyArtsPathologyAuditory PhysiologyAuditory ResearchHuman HearingTmc1 GeneMedicineNeurogeneticsHearing Loss
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