Johnson, Colin P <br/><br/>
Pathogenic proline mutation in the linker between spectrin repeats: disease caused by spectrin unfolding.  [electronic resource] 

 -  Blood  Apr 2007 
 - 3538-43 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0006-4971 
<br/><br/><label>Standard No.: </label>10.1182/blood-2006-07-038588  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Elliptocytosis, Hereditary--genetics<br/>Humans<br/>Mutation, Missense<br/>Proline--chemistry<br/>Protein Folding<br/>Spectrin--chemistry<br/>Spherocytosis, Hereditary--genetics