Prevalence and Clinical Features of Hearing Loss Patients with CDH23 Mutations: A Large Cohort Study

Lignende værker

• Mutation spectrum and genotype–phenotype correlation of hearing loss patients caused by SLC26A4 mutations in the Japanese: a large cohort study
  af: Miyagawa, Maiko, et al.
  Udgivet: (2014)
• Patients with CDH23 mutations and the 1555A>G mitochondrial mutation are good candidates for electric acoustic stimulation (EAS)
  af: Usami, Shin-Ichi, et al.
  Udgivet: (2012)
• Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss Patients
  af: Mori, Kentaro, et al.
  Udgivet: (2016)
• Sensorineural hearing loss and mild cardiac phenotype caused by an EYA4 mutation
  af: Abe, Satoko, et al.
  Udgivet: (2018)
• Mutational Spectrum and Clinical Features of Patients with LOXHD1 Variants Identified in an 8074 Hearing Loss Patient Cohort
  af: Maekawa, Karuna, et al.
  Udgivet: (2019)