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Khalsa Al Lamki
Khalsa Al Lamki
Sultan Qaboos University
Genetics
Hearing loss
Biology
Exome sequencing
Gene
3
Papers
16
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0
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LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss
2018
European Journal of Medical Genetics
Ahmed Al-Amri
Abeer Al Saegh
Watfa Al-Mamari
Mohammed E. El-Asrag
Mohammed Nasser Al-Kindi
Mazin Al Khabouri
Nadia Al-Wardy
Khalsa Al Lamki
Ahlam Gabr
Ahmed Idris
Chris F. Inglehearn
Steven J. Clapcote
Manir Ali
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In silico Analysis of a Causative Mutation in Cadherin-23 Gene Identified in an Omani Family with Hearing Loss
2018
World Academy of Science, Engineering and Technology, International Journal of Biomedical and Biological Engineering
Mohammed Nasser Al-Kindi
Mazin Al Khabouri
Khalsa Al Lamki
Tommasso Pappuci
Giovani Romeo
Nadia Al-Wardy
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