High Frequency of the p.R34X Mutation in the TMC1 Gene Associated with Nonsyndromic Hearing Loss Is Due to Founder Effects

di Saïd, Mariem Ben, Hmani-Aifa, Mounira, Amar, Imen, Baig, Shahid Mahmood, Mustapha, Mirna, Delmaghani, Sedigheh, Tlili, Abdelaziz, Ghorbel, Abdelmonem, Ayadi, Hammadi, Van Camp, Guy, Smith, Richard J.H., Tekin, Mustafa, Masmoudi, Saber
Pubblicazione 2010