High frequency of the p.R34X mutation in the TMC1 gene associated with nonsyndromic hearing loss is due to founder effects

  • Mariem Ben Saïd
  • , Mounira Hmani-Aifa
  • , Imen Amar
  • , Shahid Mahmood Baig
  • , Mirna Mustapha
  • , Sedigheh Delmaghani
  • , Abdelaziz Tlili
  • , Abdelmonem Ghorbel
  • , Hammadi Ayadi
  • , Guy Van Camp
  • , Richard J.H. Smith
  • , Mustafa Tekin
  • , Saber Masmoudi

Research output: Contribution to journal › Article › peer-review

42 Citations (Scopus)

Fingerprint

Dive into the research topics of 'High frequency of the p.R34X mutation in the TMC1 gene associated with nonsyndromic hearing loss is due to founder effects'. Together they form a unique fingerprint.

Biochemistry, Genetics and Molecular Biology

Neuroscience