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Mutations at position 7445 in the precursor of mitochondrial tRNA(Ser(UCN)) gene in three maternal Chinese pedigrees with sensorineural hearing loss.
Chen J, Yuan H, Lu J, Liu X, Wang G, Zhu Y, Cheng J, Wang X, Han B, Yang L, Yang S, Yang A, Sun Q, Kang D, Zhang X, Dai P, Zhai S, Han D, Young WY, Guan MX. Chen J, et al. Among authors: zhang x. Mitochondrion. 2008 Sep;8(4):285-92. doi: 10.1016/j.mito.2008.05.002. Epub 2008 May 23. Mitochondrion. 2008. PMID: 18639500
Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss.
Yuan H, Qian Y, Xu Y, Cao J, Bai L, Shen W, Ji F, Zhang X, Kang D, Mo JQ, Greinwald JH, Han D, Zhai S, Young WY, Guan MX. Yuan H, et al. Among authors: zhang x. Am J Med Genet A. 2005 Oct 1;138A(2):133-40. doi: 10.1002/ajmg.a.30952. Am J Med Genet A. 2005. PMID: 16152638 Free PMC article.
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: zhang r, zhang x. 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: zhang x. 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.
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