Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families - Concepedia

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Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families

21

Citations

31

References

2017

Year

Sara Salime, Majida Charif, Amale Bousfiha, Soukaina Elrharchi, Amina Bakhchane, Hicham Charoute, Mostafa Kabine, Khalid Snoussi, Guy Lenaers, Abdelhamid Barakat

International Journal of Pediatric Otorhinolaryngology

Homozygous MutationsMyo15a GenesGenetic DisorderGeneticsAudiologyPathologyMolecular GeneticsCochlear DevelopmentHuman HearingMoroccan FamiliesArtsMedicineHearing Loss

References

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