Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Saida Benarab"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b520ebc61e08e77e5a44e9222355385
https://doi.org/10.1093/hmg/6.12.2173
https://doi.org/10.1093/hmg/6.12.2173
Autor:
Christine Petit, Sébastien Chardenoux, Mohamed Drira, A. Belkahia, Christophe Vincent, Jacqueline Levilliers, Saida Benarab, Nabiha Salem, Viki Kalatzis, Catherine Dodé, Elie El Zir, Hammadi Ayadi, Sandrine Marlin, Sylvie Compain, Jacques Loiselet, Christophe Place, Hassan Chaib
Publikováno v:
Annales de l'Institut Pasteur / Actualités. 6:304-309
Les deficits hereditaires de l'audition constituent l'atteinte sensorielle la plus frequente chez l'enfant. Certains sont associes a d'autres symptomes (surdites syndromiques). La plupart se presentent comme un deficit sensoriel isole. Ces derniers,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d705af0ea240b61dade96028d29e99ef
https://doi.org/10.1016/0924-4204(96)83388-9
https://doi.org/10.1016/0924-4204(96)83388-9