Latour, Philippe <br/><br/>
A major determinant for binding and aminoacylation of tRNA(Ala) in cytoplasmic Alanyl-tRNA synthetase is mutated in dominant axonal Charcot-Marie-Tooth disease.  [electronic resource] 

 -  American journal of human genetics  Jan 2010 
 - 77-82 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1537-6605 
<br/><br/><label>Standard No.: </label>10.1016/j.ajhg.2009.12.005  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Alanine-tRNA Ligase--genetics<br/>Amino Acid Sequence<br/>Aminoacylation<br/>Axons--metabolism<br/>Charcot-Marie-Tooth Disease--genetics<br/>Child<br/>Cohort Studies<br/>Cytoplasm--metabolism<br/>Genes, Dominant<br/>Humans<br/>Lod Score<br/>Middle Aged<br/>Molecular Sequence Data<br/>Mutation<br/>Pedigree<br/>Sequence Homology, Amino Acid