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Whole exome sequencing identifies rare coding variants in novel human-mouse ortholog genes in African individuals diagnosed with non-syndromic hearing impairment
Oluwole, Oluwafemi G, Esoh, Kevin K, Wonkam-Tingang, Edmond, Manyisa, Noluthando, Noubiap, Jean Jacques, Chimusa, Emile R, Wonkam, AmbroiseJournal:
Experimental Biology and Medicine
DOI:
10.1177/1535370220960388
Date:
September, 2020
File:
PDF, 1.04 MB
2020