Related Articles
Mitochondrial tRNAIle A4317G mutation may be associated with hearing impairment in a Han Chinese family
The mitochondrial transfer RNAAsp A7551G mutation may contribute to the clinical expression of deafness associated with the A1555G mutation in a pedigree with hearing impairment
Analysis of mitochondrial A1555G mutation in infants with hearing impairment
Molecular analysis of mitochondrial gene mutations in Korean patients with nonsyndromic hearing loss
Gene mutation analysis and genetic counseling for patients with non‑syndromic hearing loss in Linyi region