Ding, Yu <br/><br/>
Mitochondrial tRNA(Glu) A14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Han Chinese family.  [electronic resource] 

 -  Journal of genetics and genomics = Yi chuan xue bao  Apr 2009 
 - 241-50 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1673-8527 
<br/><br/><label>Standard No.: </label>10.1016/S1673-8527(08)60111-3  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Asian People--ethnology<br/>Base Sequence<br/>Connexin 26<br/>Connexins--genetics<br/>Deafness--ethnology<br/>Female<br/>Genetic Variation<br/>Humans<br/>Male<br/>Middle Aged<br/>Mitochondria--chemistry<br/>Mitochondrial Proteins--genetics<br/>Nucleic Acid Conformation<br/>Pedigree<br/>Phenotype<br/>Point Mutation<br/>RNA, Ribosomal--chemistry<br/>RNA, Transfer, Gly--chemistry<br/>tRNA Methyltransferases--genetics