Related Overviews


More Like This

Show all results sharing this subject:

  • Chemistry


Show Summary Details

Quick Reference

or (Brit.)

a rare autosomalrecessive disorder in which plasma ceruloplasmin is severely deficient, characterized by neurological abnormalities and systemic hemosiderosis. Any of at least six mutations in a locus at 3q21‐q24 can cause the disease.


Subjects: Chemistry.

Reference entries

Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.