The mitochondrial tRNA(Ala) T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing loss - Han, Dongyi; Dai, Pu; Zhu, Qingwen; Liu, Xin; Huang, Deliang; Yuan, Yongyi; Yuan, Huijun; Wang, Xinjian; Qian, Yaping; Young, Wie-Yen; Guan, Min-Xin (Biochemical and biophysical research communications, 2007)
Keywords: Adolescent; Asian Continental Ancestry Group; Family - ethnology; Female; Genetic Predisposition to Disease - genetics; Genetic Variation - genetics; Hearing Loss - genetics; Heterozygote; Humans; Male; Mutation; Pedigree; Phenotype; RNA - genetics; RNA, Ribosomal - genetics; RNA, Transfer - genetics