Search Results - "Kroll, Charles A"

  • Showing 1 - 3 results of 3
Refine Results
  1. 1
  2. 2

    Retrospective determination of ceruloplasmin in newborn screening blood spots of patients with Wilson disease by Kroll, Charles A., Ferber, Matt J., Dawson, Brian D., Jacobson, Robert M., Mensink, Kara A., Lorey, Fred, Sherwin, John, Cunningham, George, Rinaldo, Piero, Matern, Dietrich, Hahn, Si Houn

    Published in Molecular genetics and metabolism (01-09-2006)
    “…Wilson disease is an autosomal recessive disorder of copper transport, caused by the reduced or absent function of the Wilson disease gene ATP7B on chromosome…”
    Get full text
    Journal Article
  3. 3