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)