Hideki Mutai
Kanagawa, Japan
Last Updated: 09/26/2026
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Found 52 publications
Clinical features of hearing loss and genotype-phenotype correlations in Alport syndrome caused by COL4A4 or COL4A5 variants.
Journal: Scientific reports
Published: July 04, 2025
Complete omission of exon 21 from Slc12a2 transcripts in mice results in hearing loss.
Journal: Scientific reports
Published: February 02, 2025
Auditory neuropathy spectrum disorder and related auditory features in patients with hearing loss associated with the MT-TS1 m.7471dup variant.
Journal: Mitochondrion
Published: December 04, 2024
Genetic landscape in undiagnosed patients with syndromic hearing loss revealed by whole exome sequencing and phenotype similarity search.
Journal: Human genetics
Published: October 18, 2024
Detailed characterization of auditory neuropathy in perrault syndrome with TWNK variants.
Journal: Auris, nasus, larynx
Published: July 08, 2024
Generation of four induced pluripotent stem cell lines (KEIUi004-A, KEIUi005-A, KEIUi006-A, and KEIUi007-A) from patients with sensorineural hearing loss with mutation in EYA4 gene.
Journal: Stem cell research
Published: March 18, 2024
Structural basis for pathogenic variants of GJB2 and hearing levels of patients with hearing loss.
Journal: BMC research notes
Published: August 15, 2023
Pax3 deficiency diminishes melanocytes in the developing mouse cochlea.
Journal: Research square
Published: June 19, 2023
Loss of Pax3 causes reduction of melanocytes in the developing mouse cochlea.
Journal: Scientific reports
Published: May 28, 2023
Apoptosis of type I spiral ganglion neuron cells in Otof-mutant mice.
Journal: Neuroscience letters
Published: November 29, 2022
Correlation between genotype and phenotype with special attention to hearing in 14 Japanese cases of NF2-related schwannomatosis.
Journal: Scientific reports
Published: September 27, 2022
Last Updated: 09/26/2026