Whole exome sequencing identifies rare coding variants in novel human-mouse ortholog genes in African individuals diagnosed with non-syndromic hearing impairment
Oluwafemi Oluwole, Kevin K. Esoh, Edmond Wonkam-Tingang, Noluthando Manyisa, Jean J. Noubiap, Emile Rugamika Chimusa, Ambroise Wonkam
Research output: Contribution to journal › Article › peer-review
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