Winston, Gavin P <br/><br/>
Copper deficiency myelopathy and subacute combined degeneration of the cord - why is the phenotype so similar?  [electronic resource] 

 -  Medical hypotheses  Aug 2008 
 - 229-36 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0306-9877 
<br/><br/><label>Standard No.: </label>10.1016/j.mehy.2008.03.027  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase--metabolism<br/>Copper--deficiency<br/>Electron Transport Complex IV--metabolism<br/>Humans<br/>Methylation<br/>Methylmalonyl-CoA Mutase--metabolism<br/>Models, Biological<br/>Models, Theoretical<br/>Nitrous Oxide--metabolism<br/>Phenotype<br/>Spinal Cord Diseases--diagnosis<br/>Subacute Combined Degeneration--diagnosis<br/>Vitamin B 12 Deficiency--complications