Henriques, Bárbara J <br/><br/>
Mutational hotspots in electron transfer flavoprotein underlie defective folding and function in multiple acyl-CoA dehydrogenase deficiency.  [electronic resource] 

 -  Biochimica et biophysica acta  Nov 2010 
 - 1070-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0006-3002 
<br/><br/><label>Standard No.: </label>10.1016/j.bbadis.2010.07.015  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine Monophosphate--metabolism<br/>Binding Sites--genetics<br/>Circular Dichroism--methods<br/>Electron-Transferring Flavoproteins--chemistry<br/>Humans<br/>Models, Molecular<br/>Multiple Acyl Coenzyme A Dehydrogenase Deficiency--genetics<br/>Mutation<br/>Protein Binding<br/>Protein Folding<br/>Protein Stability<br/>Protein Structure, Tertiary<br/>Spectrophotometry, Ultraviolet--methods<br/>Temperature