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Mapping of the otogelin gene (OTGN) to mouse Chromosome 7 and human Chromosome 11p14.3: a candidate for human autosomal recessive nonsyndromic deafness DFNB18

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Authors and Affiliations

  1. Unité de Génétique des Déficits Sensoriels, CNRS URA 1968, Institut Pasteur, 25 rue du Dr Roux, 75724, Paris Cedex 15, France, , , , , , FR

    Martine Cohen-Salmon & Christine Petit

  2. Unité de Génétique Médicale et Développement, INSERM U406, Faculté de Médecine, 27 boulevard Jean Moulin, 13385 Marseille Cedex 05, France, , , , , , FR

    Marie-Geneviève Mattei

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  1. Martine Cohen-Salmon
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  2. Marie-Geneviève Mattei
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  3. Christine Petit
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Received: 6 October 1998 / Accepted: 30 December 1998

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Cohen-Salmon, M., Mattei, MG. & Petit, C. Mapping of the otogelin gene (OTGN) to mouse Chromosome 7 and human Chromosome 11p14.3: a candidate for human autosomal recessive nonsyndromic deafness DFNB18. 10, 520–522 (1999). https://doi.org/10.1007/s003359901033

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  • DOI: https://doi.org/10.1007/s003359901033

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