In silico analysis of a novel causative mutation in Cadherin23 gene identified in an Omani family with hearing loss

por Al-Kindi, Mohammed Nasser, Al-Khabouri, Mazin Jawad, Al-Lamki, Khalsa Ahmad, Palombo, Flavia, Pippucci, Tommaso, Romeo, Giovanni, Al-Wardy, Nadia Mohammed
Publicado 2020