Aceruloplasminemia, an iron metabolic disorder
Author:
Publisher
Wiley
Subject
Neurology (clinical),General Medicine,Pathology and Forensic Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1440-1789.2003.00521.x/fullpdf
Reference18 articles.
1. Familial apoceruloplasmin deficiency associated with blepharospasm and retinal degeneration
2. Hereditary ceruloplasmin deficiency with hemosiderosis: A clinicopathological study of a japanese family
3. Late Onset Diabetes Mellitus in Patients with Hereditary Aceruloplasminemia.
4. A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans
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