ARNSD; X-linked deafness - Abram Vore
DFNA26
DFNB7/11
Pendrin Syndrome - Tao Yang
Mutation
screening for GJB2(protein-connexin 26), SLC26A4 and EYA1(protein-eyes absent
1) - Carla Nishimura
Otosclerosis
DFNB1 locus - Hela Azaiez
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