✦ LIBER ✦

The mitochondrial tRNAAla 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

✍ Scribed by Dongyi Han; Pu Dai; Qingwen Zhu; Xin Liu; Deliang Huang; Yongyi Yuan; Huijun Yuan; Xinjian Wang; Yaping Qian; Wie-Yen Young; Min-Xin Guan

Book ID: 116294786
Publisher: Elsevier Science
Year: 2007
Tongue: English
Weight: 699 KB
Volume: 357
Category: Article
ISSN: 0006-291X
DOI: 10.1016/j.bbrc.2007.03.199

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

88 Variants in mitochondrial tRNAs may i

88 Variants in mitochondrial tRNAs may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G and C1494T mutations in Chinese families with hearing loss

✍ Min-Xin Guan; Wie-Yen Young; Lidong Zhao; Yaping Qian; Ronghua Li; Jing Chen; Pu 📂 Article 📅 2007 🏛 Elsevier Science 🌐 English ⚖ 47 KB

Mitochondrial ND5 T12338C, tRNACys T5802

Mitochondrial ND5 T12338C, tRNACys T5802C, and tRNAThr G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees

✍ Bobei Chen; Dongmei Sun; Li Yang; Chuqin Zhang; Aifen Yang; Yi Zhu; Jianyue Zhao 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 240 KB 👁 1 views

Mitochondrial tRNAGlu A14693G variant ma

Mitochondrial tRNAGlu A14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Han Chinese family

✍ Yu Ding; Yongyan Li; Junyan You; Li Yang; Bobei Chen; Jianxin Lu; Min-Xin Guan 📂 Article 📅 2009 🏛 Elsevier 🌐 Chinese ⚖ 545 KB

Clinical and molecular analysis of a fou

Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation

✍ Qiuju Wang; Qing-Zhong Li; Dongyi Han; Yali Zhao; Lidong Zhao; Yaping Qian; Hu Y 📂 Article 📅 2006 🏛 Elsevier Science 🌐 English ⚖ 255 KB

Mitochondrial COX2 G7598A Mutation May H

Mitochondrial COX2 G7598A Mutation May Have a Modifying Role in the Phenotypic Manifestation of Aminoglycoside Antibiotic-Induced Deafness Associated with 12S rRNA A1555G Mutation in a Han Chinese Pedigree

✍ Chen, Tianbin; Liu, Qicai; Jiang, Ling; Liu, Can; Ou, Qishui 📂 Article 📅 2013 🏛 Mary Ann Liebert 🌐 English ⚖ 367 KB

Variants in mitochondrial tRNAGlu, tRNAA

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

✍ Wie-Yen Young; Lidong Zhao; Yaping Qian; Ronghua Li; Jing Chen; Huijun Yuan; Pu 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 269 KB 👁 2 views