Please use this identifier to cite or link to this item:
http://www.edream.ma:8080/jspui/handle/123456789/1471| Title: | Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families |
| Authors: | Salime, Sara Charif, Majida Bousfiha, Amale Elrharchi, Soukaina Bakhchane, Amina Charoute, Hicham Kabine, Mostafa Snoussi, Khalid Lenaers, Guy Barakat, Abdelhamid |
| Keywords: | PJVK MYO15A Hearing Loss Whole Exome Sequencing Morocco |
| Issue Date: | 2017 |
| Publisher: | International Journal of Pediatric Otorhinolaryngology |
| URI: | http://dream:8080/jspui/handle/123456789/1471 |
| Appears in Collections: | Science & Technology |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families.pdf | 1.55 MB | Adobe PDF | View/Open |
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