PreprintAll rights reservedbioRxiv
KDM6A Haploinsufficiency Is Insufficient to Disrupt Cochlear Structure and Auditory Function in Mouse Models of Kabuki Syndrome Type 2
- 1University of Florida
Related
- Slc16a5 (MCT6) Knockout Induces Sex-Dependent Changes in Auditory Function, Hair Cell Viability and Cochlear Transcriptomic Programs in the Mouse
- Multichannel optical cochlear implants enable spectrally distinct auditory activity
- Top-down inferior colliculus signals engage unipolar brush cell circuits in the dorsal cochlear nucleus of the mouse auditory system
- Temporal Auditory Resolution, Timed Motor Responses to Auditory Cues, and Phonological Processing in Swedish Children with Cochlear Implants and Normal Hearing Peers.
- Remote analysis of auditory performance in cochlear implant users using a new tool: remote check.
BibTeX
@misc{shimizu2026kdm6a,
title = {{KDM6A Haploinsufficiency Is Insufficient to Disrupt Cochlear Structure and Auditory Function in Mouse Models of Kabuki Syndrome Type 2}},
author = {Y. Shimizu and S. Wakamori and L. Smith and G. Behnammanesh and Y. Honkura and J. Suzuki and J. E. Bird and Y. Katori and S. Someya},
howpublished = {bioRxiv},
year = {2026},
month = oct,
doi = {10.64898/2026.10.09.757851},
url = {https://www.biorxiv.org/content/10.64898/2026.10.09.757851v1},
}
RIS
TY - UNPB
TI - KDM6A Haploinsufficiency Is Insufficient to Disrupt Cochlear Structure and Auditory Function in Mouse Models of Kabuki Syndrome Type 2
AU - Y. Shimizu
AU - S. Wakamori
AU - L. Smith
AU - G. Behnammanesh
AU - Y. Honkura
AU - J. Suzuki
AU - J. E. Bird
AU - Y. Katori
AU - S. Someya
PY - 2026
DA - 2026/10/09
PB - bioRxiv
DO - 10.64898/2026.10.09.757851
UR - https://www.biorxiv.org/content/10.64898/2026.10.09.757851v1
ER -