Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families
| Autor: | Salime, Sara, Charif, Majida, Bousfiha, Amale, Elrharchi, Soukaina, Bakhchane, Amina, Charoute, Hicham, Kabine, Mostafa, Snoussi, Khalid, Lenaers, Guy, Barakat, Abdelhamid |
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| Zdroj: | In International Journal of Pediatric Otorhinolaryngology October 2017 101:25-29 |
| Databáze: | ScienceDirect |
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