LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss
Titel:
LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss
Auteur:
Al-Amri, Ahmed H. Al Saegh, Abeer Al-Mamari, Watfa El-Asrag, Mohammed E. Al-Kindi, Mohammed N. Al Khabouri, Mazin Al Wardy, Nadia Al Lamki, Khalsa Gabr, Ahlam Idris, Ahmed Inglehearn, Chris F. Clapcote, Steven J. Ali, Manir