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Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus. |
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| Authors: | E Verpy S Masmoudi I Zwaenepoel M Leibovici T P Hutchin I Del Castillo S Nouaille S Blanchard S Lainé J L Popot F Moreno R F Mueller C Petit |
| Institution: | Unité de Génétique des Déficits Sensoriels, CNRS URA 1968, Institut Pasteur, 25 rue du Dr. Roux, 75724 Paris cedex 15, France. |
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