论文信息 - LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss. - 字舞流文

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

C. Inglehearn | S. Clapcote | Manir Ali | Watfa S Al-Mamari | Mazin Al Khabouri | M. El-Asrag | M. Al-Kindi | A. Al-Amri | A. Idris | N. Al Wardy | A. Gabr | Abeer Al Saegh | Khalsa Al Lamki