Lübke, T <br/><br/>
Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiency.  [electronic resource] 

 -  Nature genetics  May 2001 
 - 73-6 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1061-4036 
<br/><br/><label>Standard No.: </label>10.1038/ng0501-73  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Biological Transport<br/>Carrier Proteins--genetics<br/>Cells, Cultured<br/>Cloning, Molecular<br/>Congenital Disorders of Glycosylation--classification<br/>Fibroblasts--cytology<br/>Genetic Complementation Test<br/>Glycosylation<br/>Guanosine Diphosphate Fucose--metabolism<br/>Humans<br/>Male<br/>Molecular Sequence Data<br/>Monosaccharide Transport Proteins<br/>Sequence Homology, Amino Acid