Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice
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DOI: 10.1073/pnas.2204084119
Abstract: Significance Molecular components of hearing in mammalians are not completely delineated. Via a genetic approach conducted in families with sensorineural hearing loss, this study presents MINAR2 as an indispensable element of hearing in humans. Similarly,… read more here.
Keywords: hearing; hair cells; humans mice; mutations minar2 ... See more keywords