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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*
*Corresponding author for this work
Research output: Contribution to journal › Article › peer-review
5
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(Scopus)