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To study the distribution characteristics of common mutations in the GJB2, SLC26A4, and mtDNA genes in children with severe or profound sensorineural hearing loss (SNHL) in southwestern China.

genetic testing and molecular biomarkers

Prevalence of Mutations in GJB2, SLC26A4, and mtDNA in Children with Severe or Profound Sensorineural Hearing Loss in Southwestern China