OSBPL2 encodes a protein of inner and outer hair cell stereocilia and is mutated in autosomal dominant hearing loss (DFNA67)

Overview of attention for article published in Orphanet Journal of Rare Diseases, February 2015

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OSBPL2 encodes a protein of inner and outer hair cell stereocilia and is mutated in autosomal... http://t.co/HYSP8o1lbn #NGS #sequencing

Hair cell stereocilia gene OSBPL2 is mutated in autosomal dominant hearing loss http://t.co/N7B6KgHd1I - new in OJRD #raredisease #deafness

OSBPL2 encodes a protein of inner and outer hair cell stereocilia and is mutated in autosomal dominant hearing... http://t.co/1A2i4DG2Mp

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