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Al-Amri, AH, Al Saegh, A, Al-Mamari, W et al. (10 more authors) (2018) LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss. European Journal of Medical Genetics. ISSN 1769-7212

This list was generated on Mon Nov 11 12:10:25 2019 GMT.