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Loryn Smith

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Open access Oct 2026

KDM6A Haploinsufficiency Is Insufficient to Disrupt Cochlear Structure and Auditory Function in Mouse Models of Kabuki Syndrome Type 2

It is suggested that partial Kdm6a loss alone is insufficient to produce a robust primary cochlear phenotype in young mice and highlight the potential contributions of non-cochlear, developmental, central, and later-onset mechanisms to hearing impairment in KS2.

Yuichi Shimizu, Shun Wakamori, Loryn Smith et al. · 0 citations

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