Associated Papers
Screening of common point-mutations and discovery of new T14727C change in mitochondrial genome of Vietnamese encephalomyopathy patients.
Truong HT et al.
Mitochondrial Dna. Part A, Dna Mapping, Sequencing, and Analysis, 2016
A rapid method for simultaneous screening of multi-gene mutations associated with hearing loss in the Korean population.
Sagong B et al.
Plos One, 2013
Prevalence of mitochondrial DNA mutations in sporadic patients with nonsyndromic sensorineural hearing loss.
Jiang H et al.
Brazilian Journal of Otorhinolaryngology, 0
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