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2. A systematic review of the monogenic causes of Non‐Syndromic Hearing Loss (NSHL) and discussion of Current Diagnosis and Treatment options
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3. Mitochondrial tRNASer(UCN) mutations associated non-syndromic sensorineural hearing loss in Chinese families
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4. Maternally transmitted nonsyndromic hearing impairment may be associated with mitochondrial tRNAAla 5601C>T and tRNALeu(CUN) 12311T>C mutations
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