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Autor:
Mohammed Grati, Pierre Bitoun, Saida Benarab, Stephen A. Wilcox, Christine Petit, Alain Joannard, Amel Boulila-Elgaied, Elie El-Zir, J Godet, Mirna Mustapha, Hans Henrik M. Dahl, Jacqueline Levilliers, Denise R. Allen-Powell, Nicholas Lench, Jacques Loiselet, Anna Middleton, Mark J. Houseman, Hammadi Ayadi, Marion A. Maw, Robert F. Mueller, Catherine Dodé, Amelia H. Osborn, Françoise Denoyelle, Dominique Weil, R. J McKinlay Gardner, Anne Aubois, Geneviève Lina-Granade, Erea Noel Garabedian, Sandrine Marlin
Publikováno v:
Human Molecular Genetics. 6:2173-2177
Prelingual non-syndromic (isolated) deafness is the most frequent hereditary sensory defect. In >80% of the cases, the mode of transmission is autosomal recessive. To date, 14 loci have been identified for the recessive forms (DFNB loci). For two of