| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8806132 | International Journal of Pediatric Otorhinolaryngology | 2018 | 5 Pages |
Abstract
These results further substantiate the genetic heterogeneity of HI, even in reportedly isolated populations. However, several families may harbor the same mutations as a result of a long history of marriages between relatives. This study has important implications for the HI molecular diagnosis strategy, and to develop genetic counseling for families originating from the Ghardaïa province of Algeria.
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Authors
Sonia Talbi, Crystel Bonnet, Zied Riahi, Farid Boudjenah, Malika Dahmani, Jean-Pierre Hardelin, Fabienne Wong Jun Tai, Malek Louha, Fatima Ammar-Khodja, Christine Petit,