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Khalsa Ahmad Al-Lamki
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Khalsa Ahmad Al-Lamki
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In silico analysis of a novel causative mutation in Cadherin23 gene identified in an Omani family with hearing loss
by
Mohammed Nasser Al-Kindi
,
Mazin Jawad Al-Khabouri
,
Khalsa
Ahmad
Al
-
Lamki
,
Flavia Palombo
,
Tommaso Pippucci
,
Giovanni Romeo
,
Nadia Mohammed Al-Wardy
Published 2020-03-01
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