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Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafness.
Dai P, Liu X, Han D, Qian Y, Huang D, Yuan H, Li W, Yu F, Zhang R, Lin H, He Y, Yu Y, Sun Q, Qin H, Li R, Zhang X, Kang D, Cao J, Young WY, Guan MX. Dai P, et al. Among authors: han d. Biochem Biophys Res Commun. 2006 Feb 3;340(1):194-9. doi: 10.1016/j.bbrc.2005.11.156. Biochem Biophys Res Commun. 2006. PMID: 16375862 Clinical Trial.
[Genotypic analysis of familial dilated vestibular aqueduct syndrome].
Dai P, Han D, Cao J, Zhai S, Kang D, Liu X, Yuan H, Zhang X, Li M, Liu L, Feng B, Yang W, Wu B. Dai P, et al. Among authors: han d. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2006 Feb;20(4):147-50. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2006. PMID: 16711435 Chinese.
Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss.
Young WY, Zhao L, Qian Y, Li R, Chen J, Yuan H, Dai P, Zhai S, Han D, Guan MX. Young WY, et al. Among authors: han d. Am J Med Genet A. 2006 Oct 15;140(20):2188-97. doi: 10.1002/ajmg.a.31434. Am J Med Genet A. 2006. PMID: 16955413
We report here on the clinical, genetic, and molecular characterization of three Han Chinese pedigrees with aminoglycoside-induced and nonsyndromic hearing loss. ...Furthermore, the T15908C mutation in the tRNA(Thr) disrupts a highly conserved A-U base-pairing at the D …
We report here on the clinical, genetic, and molecular characterization of three Han Chinese pedigrees with aminoglycoside-induced an …
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