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This article provides historical context about the characterization of GLP1 and extensively reviews its physiological role

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The inbred mouse model of C57BL/6J background has shown high-frequency hearing loss and cochlea basal turn cytostructural degeneration from 6-months of age, in part caused by the presence of the ARHL susceptibility allele ( Ahl ), which encodes for caderhin 23 expressed in the stereocilia of HCs (Zheng et al., 1999)

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