LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss

Ahmed H. Al-Amri, Abeer Al Saegh, Watfa Al-Mamari, Mohammed E. El-Asrag, Mohammed N. Al-Kindi, Mazin Al Khabouri, Nadia Al Wardy, Khalsa Al Lamki, Ahlam Gabr, Ahmed Idris, Chris F. Inglehearn, Steven J. Clapcote, Manir Ali^*