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Prestin gene therapy is a **preclinical inner-ear gene therapy concept** intended to restore cochlear outer hair cell function by delivering a functional copy of **SLC26A5**, the gene encoding prestin, a voltage-sensitive motor protein that drives outer hair cell electromotility and cochlear amplification. The therapeutic rationale is that replacement of defective or absent prestin should re-establish outer hair cell mechanical amplification and thereby improve hearing in **SLC26A5-related hereditary hearing loss**. Published research supports this concept in animal models, but there is no clearly established, uniquely named clinical drug product, brand, or code designation identifiable from the queried term alone.
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