Mitochondrial tRNAGlu 14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Hah Chinese family

机标关键词：family pedigree、Chinese、hearing loss、protein synthesis、characterization、12S rRNA、conventional、tRNA、analysis、high、set、Han

所属期刊栏目：36

分类号：Q3(遗传学)

资助基金：This work was supported by the Public Health Service grantsRO1DC05230;ROlDC07696;from the National Institute on Deafness and Other Communication Disorders, and grants from the National Basic Research Priorities Program of China2004CCA02200;the Ministry of Science and Technology of Zhejiang Province2007G50G2090026;Zhejiang Provincial Program for the Cultivation of High-level Innovative Health talents to M.X.G

在线出版日期：2010-07-12（万方平台首次上网日期，不代表论文的发表时间）

页码：241-250