Richard, Eva <br/><br/>
Congenital disorder of glycosylation Ia: new differentially expressed proteins identified by 2-DE.  [electronic resource] 

 -  Biochemical and biophysical research communications  Feb 2009 
 - 267-71 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1090-2104 
<br/><br/><label>Standard No.: </label>10.1016/j.bbrc.2008.12.036  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Carrier Proteins--biosynthesis<br/>Child<br/>Child, Preschool<br/>Electrophoresis, Gel, Two-Dimensional<br/>Female<br/>Fibrin--analysis<br/>Fibrinogen--analysis<br/>Glycoproteins--biosynthesis<br/>Glycosylation<br/>Humans<br/>Isoelectric Focusing<br/>Metabolism, Inborn Errors--blood<br/>Protein Biosynthesis<br/>Proteins--analysis<br/>Proteome--analysis<br/>Proteomics<br/>Serum--metabolism<br/>Serum Albumin--biosynthesis<br/>Serum Albumin, Human<br/>Transferrin--analysis<br/>alpha 1-Antitrypsin--biosynthesis<br/>alpha-Macroglobulins--analysis