References
- Morton CC, Nance WE. Newborn hearing screening – a silent revolution. N Engl J Med 2006;354:2151–64.
- Schapira AH. Mitochondrial disease. Lancet 2006;368:70–82.
- Uchida Y, Sugiura S, Ando F, Nakashima T, Shimokata H. Hearing impairment risk and interaction of folate metabolism related gene polymorphisms in an aging study. BMC Med Genet 2011;12:35.
- Furuta T, Teranishi M, Uchida Y, Nishio N, Kato K, Otake H, Association of interleukin-1 gene polymorphisms with sudden sensorineural hearing loss and Meniere's disease. Int J Immunogenet 2011;38:249–54.
- Noguchi Y, Yashima T, Ito T, Sumi T, Tsuzuku T, Kitamura K. Audiovestibular findings in patients with mitochondrial A1555G mutation. Laryngoscope 2004;114:344–8.
- Tamagawa Y, Kitamura K, Hagiwara H, Ishida T, Nishizawa M, Saito T, Audiologic findings in patients with a point mutation at nucleotide 3,243 of mitochondrial DNA. Ann Otol Rhinol Laryngol 1997;106:338–42.
- Kato T, Nishigaki Y, Noguchi Y, Ueno H, Hosoya H, Ito T, Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss. J Hum Genet 2010;55:147–54.
- Tanaka M, Cabrera VM, Gonzalez AM, Larruga JM, Takeyasu T, Fuku N, Mitochondrial genome variation in eastern Asia and the peopling of Japan. Genome Res 2004;14:1832–50.
- Dunbar SA. Applications of Luminex xMAP technology for rapid, high-throughput multiplexed nucleic acid detection. Clin Chim Acta 2006;363:71–82.
- Fuku N, Park KS, Yamada Y, Nishigaki Y, Cho YM, Matsuo H, Mitochondrial haplogroup N9a confers resistance against type 2 diabetes in Asians. Am J Hum Genet 2007;80:407–15.
- Yao YG, Kong QP, Bandelt HJ, Kivisild T, Zhang YP. Phylogeographic differentiation of mitochondrial DNA in Han Chinese. Am J Hum Genet 2002;70:635–51.
- Ballana E, Morales E, Rabionet R, Montserrat B, Ventayol M, Bravo O, Mitochondrial 12S rRNA gene mutations affect RNA secondary structure and lead to variable penetrance in hearing impairment. Biochem Biophys Res Commun 2006;341:950–7.
- Lu J, Li Z, Zhu Y, Yang A, Li R, Zheng J, Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss. Mitochondrion 2010;10:380–90.
- Li R, Xing G, Yan M, Cao X, Liu XZ, Bu X, Cosegregation of C-insertion at position 961 with the A1555G mutation of the mitochondrial 12S rRNA gene in a large Chinese family with maternally inherited hearing loss. Am J Med Genet A 2004;124A:113–17.
- Chen B, Sun D, Yang L, Zhang C, Yang A, Zhu Y, Mitochondrial ND5 T12338C, tRNA(Cys) T5802C, and tRNA(Thr) G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees. Am J Med Genet A 2008;146A:1248–58.
- Murakami H, Ota A, Simojo H, Okada M, Ajisaka R, Kuno S. Polymorphisms in control region of mtDNA relates to individual differences in endurance capacity or trainability. Jpn J Physiol 2002;52:247–56.
- Wang H, Hiatt WR, Barstow TJ, Brass EP. Relationships between muscle mitochondrial DNA content, mitochondrial enzyme activity and oxidative capacity in man: alterations with disease. Eur J Appl Physiol Occup Physiol 1999;80:22–7.
- Xing G, Chen Z, Cao X. Mitochondrial rRNA and tRNA and hearing function.. Cell Res 2007;17:227–39.
- Uchida Y, Sugiura S, Nakashima T, Ando F, Shimokata H. Endothelin-1 gene polymorphism and hearing impairment in elderly Japanese. Laryngoscope 2009;119:938–43.
- Alexe G, Satya RV, Seiler M, Platt D, Bhanot T, Hui S, PCA and clustering reveal alternate mtDNA phylogeny of N and M clades. J Mol Evol 2008;67:465–87.