Publication | Open Access
Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2
51
Citations
35
References
2016
Year
Genetic DisorderGeneticsAudiologyAuditory PhysiologyRare Missense VariantsMedical GeneticsAuditory ResearchAuditory ScienceHuman HearingArtsMedicineAuditory SystemHearing Loss
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