Exploration of molecular genetic etiology for Korean cochlear implantees with severe to profound hearing loss and its implication

Overview of attention for article published in Orphanet Journal of Rare Diseases, November 2014

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Over 50% of severe-to-profound hearing loss cases in a #Korea study were Mendelian disorders of known #deafness genes http://t.co/KbVJLLu0KP

Exploration of molecular genetic etiology for Korean cochlear implantees with severe to profound hearing loss ... http://t.co/v1dTgJFhpH

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