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Abbreviation : HCD
Long Form : hereditary ceruloplasmin deficiency
No. Year Title Co-occurring Abbreviation
2000 A novel mutation of the ceruloplasmin gene in a patient with heteroallelic ceruloplasmin gene mutation (HypoCPGM). Cp, PCR
1999 A case of hereditary ceruloplasmin deficiency with iron deposition in the brain associated with chorea, dementia, diabetes mellitus and retinal pigmentation: administration of fresh-frozen human plasma. FFP
1999 Hereditary ceruloplasmin deficiency increases advanced glycation end products in the brain. ---
1997 Islet changes in hereditary ceruloplasmin deficiency. DM
1995 A nonsense mutation of the ceruloplasmin gene in hereditary ceruloplasmin deficiency with diabetes mellitus. Cp, DM, PCR