Items where authors include "Al Lamki, K"
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Article
Al-Amri, AH, Al Saegh, A, Al-Mamari, W et al. (10 more authors) (2019) LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss. European Journal of Medical Genetics, 62 (12). 103592. ISSN 1769-7212