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Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families. [electronic resource] by
- Salime, Sara
- Charif, Majida
- Bousfiha, Amale
- Elrharchi, Soukaina
- Bakhchane, Amina
- Charoute, Hicham
- Kabine, Mostafa
- Snoussi, Khalid
- Lenaers, Guy
- Barakat, Abdelhamid
Producer: 20171023
In:
International journal of pediatric otorhinolaryngology vol. 101
Availability: No items available.
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