Saitama Medical University · Faculty of Medicine / Graduate School of Medicine · 教授

Research keywordshearing loss genetics・perilymphatic fistula・delayed endolymphatic hydrops・MYO6 variants・OTOF-related hearing loss・ACTG1 mutations・inner ear anomalies

This is a public-data preview. Personalized fit, contact angles, and saved workflows require sign-in.

• Detailed clinical features and genotype-phenotype correlation in an OTOF-related hearing loss cohort in Japan
• 両側急性感音難聴を呈した内耳梅毒の1例
• OTOF mutation analysis with massively parallel DNA sequencing in 2,265 Japanese sensorineural hearing loss patients
• A 14-year nationwide epidemiological analysis of delayed endolymphatic hydrops in Japan

• Official profile
• ORCID