D. Yan, M. Tekin, S. Blanton, and X. Liu, Next-Generation Sequencing in Genetic Hearing Loss, Genetic Testing and Molecular Biomarkers, vol.17, issue.8, pp.581-587, 2013.
DOI : 10.1089/gtmb.2012.0464

F. Denoyelle, M. S. Weil, D. Moatti, L. Chauvin, and P. , Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling, The Lancet, vol.353, issue.9161, pp.1298-1303, 1999.
DOI : 10.1016/S0140-6736(98)11071-1

A. Sirmaci, Y. Edwards, H. Akay, and M. Tekin, Challenges in Whole Exome Sequencing: An Example from Hereditary Deafness, PLoS ONE, vol.16, issue.2, p.32000, 2012.
DOI : 10.1371/journal.pone.0032000.s001

O. Diaz-horta, D. Duman, J. Foster, A. Sirmaci, and M. Gonzalez, Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss, PLoS ONE, vol.13, issue.11, p.50628, 2012.
DOI : 10.1371/journal.pone.0050628.s003

H. Woo, H. Park, J. Baek, M. Park, and U. Kim, Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families, BMC Medical Genetics, vol.119, issue.4, p.72, 2013.
DOI : 10.1002/lary.20116

C. Bonnet, M. Louha, N. Loundon, N. Michalski, and E. Verpy, Biallelic nonsense mutations in the otogelin-like gene (OTOGL) in a child affected by mild to moderate hearing impairment, Gene, vol.527, issue.2, pp.537-540, 2013.
DOI : 10.1016/j.gene.2013.06.044

S. Delmaghani, A. Aghaie, N. Michalski, C. Bonnet, and D. Weil, Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness, Human Molecular Genetics, vol.21, issue.17, pp.3835-3844, 2012.
DOI : 10.1093/hmg/dds212

URL : https://hal.archives-ouvertes.fr/pasteur-01472843

S. Miller, D. Dykes, and H. Polesky, A simple salting out procedure for extracting DNA from human nucleated cells, Nucleic Acids Research, vol.16, issue.3, p.1215, 1988.
DOI : 10.1093/nar/16.3.1215

S. Ishida, F. Picard, R. G. Noe, E. Achaz, and G. , Mutations of DEPDC5 cause autosomal dominant focal epilepsies, Nature Genetics, vol.10, issue.5, pp.552-555, 2013.
DOI : 10.1038/ng.876

Z. Riahi, H. Chahed, H. Jaafoura, R. Zainine, and O. Messaoud, A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian families, International Journal of Pediatric Otorhinolaryngology, vol.77, issue.9, pp.1485-1488, 2013.
DOI : 10.1016/j.ijporl.2013.06.015

URL : https://hal.archives-ouvertes.fr/pasteur-00861211

Z. Riahi, H. Hammami, H. Ouragini, H. Messai, and R. Zainine, Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss, Gene, vol.525, issue.1, pp.1-4, 2013.
DOI : 10.1016/j.gene.2013.04.078

URL : https://hal.archives-ouvertes.fr/pasteur-00861409

Z. Riahi, R. Zainine, Y. Mellouli, R. Hannachi, and Y. Bouyacoub, Compound heterozygosity for dominant and recessive GJB2 mutations in a Tunisian family and association with successful cochlear implant outcome, International Journal of Pediatric Otorhinolaryngology, vol.77, issue.9, 2013.
DOI : 10.1016/j.ijporl.2013.06.013

URL : https://hal.archives-ouvertes.fr/pasteur-00860772

A. Wang, Y. Liang, R. Fridell, F. Probst, and E. Wilcox, Association of Unconventional Myosin MYO15 Mutations with Human Nonsyndromic Deafness DFNB3, Science, vol.280, issue.5368, pp.1447-1451, 1998.
DOI : 10.1126/science.280.5368.1447

I. Belyantseva, E. Boger, S. Naz, G. Frolenkov, and J. Sellers, Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia, Nature Cell Biology, vol.7, issue.2, pp.148-156, 2005.
DOI : 10.1523/JNEUROSCI.1279-04.2004

H. Belguith, M. Aifa-hmani, H. Dhouib, M. Said, and M. Mosrati, Associated with Hearing Loss and Further Suggestion for Two Distinctive Genes on This Locus, Genetic Testing and Molecular Biomarkers, vol.13, issue.1, pp.147-151, 2009.
DOI : 10.1089/gtmb.2008.0077

N. Liburd, M. Ghosh, S. Riazuddin, S. Naz, and S. Khan, Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome, Human Genetics, vol.109, issue.5, pp.535-541, 2001.
DOI : 10.1007/s004390100604

T. Yano, A. Ichinose, S. Nishio, Y. Kobayashi, and H. Sato, A Novel Mutation of MYO15A Associated with Hearing Loss in a Japanese Family, Journal of Clinical Case Reports, 2013.

Z. Ahmed, S. Masmoudi, E. Kalay, I. Belyantseva, and M. Mosrati, Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans, Nature Genetics, vol.12, issue.11, pp.1335-1340, 2008.
DOI : 10.1038/ng.245

X. Du, M. Schwander, E. Moresco, P. Viviani, and C. Haller, A catechol-O-methyltransferase that is essential for auditory function in mice and humans, Proceedings of the National Academy of Sciences, vol.105, issue.38, pp.14609-14614, 2008.
DOI : 10.1073/pnas.0807219105

M. Charif, S. Bounaceur, O. Abidi, H. Nahili, and H. Rouba, The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population, Molecular Biology Reports, vol.217, issue.8, pp.11011-11016, 2012.
DOI : 10.1007/s11033-012-2003-3

B. Said, M. Hmani-aifa, M. Amar, I. Baig, S. Mustapha et al., Gene Associated with Nonsyndromic Hearing Loss Is Due to Founder Effects, Genetic Testing and Molecular Biomarkers, vol.14, issue.3, pp.307-311, 2010.
DOI : 10.1089/gtmb.2009.0174

A. Sirmaci, D. Duman, H. Ozturkmen-akay, S. Erbek, and A. Incesulu, Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: a report of five novel mutations, 2009.

S. Kitajiri, R. Mcnamara, T. Makishima, T. Husnain, and A. Zafar, mutations causing DFNB7/B11 deafness in Pakistan, Clinical Genetics, vol.4, issue.1, pp.546-550, 2007.
DOI : 10.1111/j.1399-0004.2007.00895.x

Y. Kawashima, G. Geleoc, K. Kurima, V. Labay, and A. Lelli, Mechanotransduction in mouse inner ear hair cells requires transmembrane channel???like genes, Journal of Clinical Investigation, vol.121, issue.12, pp.4796-4809, 2011.
DOI : 10.1172/JCI60405DS1

L. Romdhane, R. Kefi, H. Azaiez, B. Halim, N. Dellagi et al., Founder mutations in Tunisia: implications for diagnosis in North Africa and Middle East, Orphanet Journal of Rare Diseases, vol.7, issue.1, p.52, 2012.
DOI : 10.1186/1750-1172-7-52

URL : https://hal.archives-ouvertes.fr/pasteur-00859423