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Front Immunol (2018) 9:1127
They identified that the risk of developing NIHL in subjects carrying TA genotype of rs4660470 was 2.197 times than the one carrying TT genotypes, suggesting that the mutant allele A of rs4660470 in KCNQ4 may be a risk factor for developing NIHL
and Awika, J., 2018
Oxidative stress, metabolic and mitochondrial abnormalities associated with autism spectrum disorder
10.1097/00005072-199111000-00008 J
Biology of diabetic neuropathy
