Copper deficiency associated with severe neurological disorder — A genetic work-up of possible mutations in copper transport proteins

✍ Scribed by Jan-Philipp Bach; Neeraj Kumar; Candan Depboylu; Carmen Noelker; Thomas Klockgether; Michael Bacher; Monika Balzer-Geldsetzer; Richard Dodel

• Book ID: 119303649
• Publisher: Elsevier Science
• Year: 2010
• Tongue: English
• Weight: 92 KB
• Volume: 291
• Category: Article
• ISSN: 0022-510X
• DOI: 10.1016/j.jns.2010.01.008