Wolf, Andreas <br/><br/>
Single base-pair substitutions at the translation initiation sites of human genes as a cause of inherited disease.  [electronic resource] 

 -  Human mutation  Oct 2011 
 - 1137-43 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/humu.21547  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>5' Flanking Region<br/>Codon, Initiator<br/>Consensus Sequence<br/>Databases, Genetic<br/>Genetic Diseases, Inborn--genetics<br/>Humans<br/>Mutation Rate<br/>Open Reading Frames<br/>Peptide Chain Initiation, Translational--genetics<br/>Point Mutation