Hypocaeruloplasminaemia with heteroallelic caeruloplasmin gene mutation: MRI of the brain

Neuroradiology

Volumn 41, Issue 3, 1999, Pages 185-187

  Daimon, M ^a   Moriai, S ^a   Susa, S ^a   Yamatani, K ^a   Hosoya, T ^a   Kato, T ^a  

^a YAMAGATA UNIVERSITY   (Japan)

Author keywords

Hereditary caeruloplasmin deficiency; Magnetic resonance imaging

Indexed keywords

CERULOPLASMIN;

AGED; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BRAIN; CASE REPORT; CERULOPLASMIN BLOOD LEVEL; DIABETES MELLITUS; FEMALE; GENE MUTATION; HUMAN; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; PUTAMEN; TREMOR;

AGED; CERULOPLASMIN; DIABETES MELLITUS; ECHO-PLANAR IMAGING; FEMALE; HUMANS; MALE; POINT MUTATION; PUTAMEN; TREMOR;

EID: 0032984353     PISSN: 00283940     EISSN: None     Source Type: Journal    
DOI: 10.1007/s002340050730     Document Type: Article

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