Screening for Mitochondrial A1555G Mutation among Assortative Mating Hearing Impaired Families in South India: Some Vital Insights

Genetic research into the mechanism of non-syndromic hearing loss (NSHL) have been hampered by a number of issues, including genetic variability, various phenotypes, consanguinity, and marriages between hearing impaired people. In numerous populations, the A1555G mutation in the MT-RNR1 gene has been found as one of the most prevalent mitochondrial mutations, and it has been…
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August 23, 2021 0