Homozygous mutations in PJVK and MYO15A genes associated with nonsyndromic hearing loss in Moroccan families

Salime S, Charif M, Bousfiha A, Elrharchi S, Bakhchane A, Charoute H, Kabine M, Snoussi K, Lenaers G. (2017) Homozygous mutations in PJVK and MYO15A genes associated with nonsyndromic hearing loss in Moroccan families. International Journal of Pediatric Otorhinolaryngology  DOI: http://dx.doi.org/10.1016/j.ijporl.2017.07.024