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Dive into the research topics of 'In silico analysis of a novel causative mutation in Cadherin23 gene identified in an Omani family with hearing loss'. Together they form a unique fingerprint.- Sort by
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Mohammed Nasser Al-Kindi, Mazin Jawad Al-Khabouri, Khalsa Ahmad Al-Lamki, Flavia Palombo, Tommaso Pippucci, Giovanni Romeo, Nadia Mohammed Al-Wardy*
Research output: Contribution to journal › Article › peer-review