Genetic load of alternations of transcription factor genes in non-syndromic deafness and the associated clinical phenotypes: experience from two tertiary referral centers

HIGHLIGHTS

  • who: Hyung Dong Jo et al. from the Department of Otorhinolaryngology-Head and Neck Surgery, Seoul National University Hospital, Seoul have published the research: Genetic Load of Alternations of Transcription Factor Genes in Non-Syndromic Deafness and the Associated Clinical Phenotypes: Experience from Two Tertiary Referral Centers, in the Journal: Biomedicines 2022, 2125 of 17/08/2022
  • what: The authors characterized the clinical phenotypes and genotypes of non-syndromic deafness caused by transcription factor (TF) gene variants one of the functional classifications of genetic hearing loss. Although in this study the authors examined the clinical . . .

     

    Logo ScioWire Beta black

    If you want to have access to all the content you need to log in!

    Thanks :)

    If you don't have an account, you can create one here.

     

Scroll to Top

Add A Knowledge Base Question !

+ = Verify Human or Spambot ?