Hereditary ceruloplasmin deficiency with hemosiderosis

Human Genetics

Volumn 97, Issue 6, 1996, Pages 755-758

  Okamoto, Nobuhiko ^a   Wada, Satoko ^b   Oga, Tatsuhide ^c   Kawabata, Yumiko ^c   Baba, Yasuto ^c   Habu, Daiki ^c   Takeda, Zenju ^c   Wada, Yoshinao ^a  

^a RESEARCH INSTITUTE FOR MATERNAL AND CHILD HEALTH   (Japan)

^b Chifune Hospital   (Japan)

^c YODOGAWA CHRISTIAN HOSPITAL   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CERULOPLASMIN; COMPLEMENTARY DNA;

ADULT; ARTICLE; BASAL GANGLION; CASE REPORT; CEREBELLAR ATAXIA; CERULOPLASMIN BLOOD LEVEL; CLINICAL FEATURE; DEMENTIA; DENTATE NUCLEUS; DIABETES MELLITUS; ENZYME DEFICIENCY; EXTRAPYRAMIDAL SYMPTOM; GENE MUTATION; HEMOSIDEROSIS; HUMAN; HUMAN TISSUE; IRON METABOLISM; MALE; NEUROLOGIC DISEASE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RED NUCLEUS; RETINA PIGMENT DEGENERATION; STOP CODON; TISSUE INJURY;

EID: 0029872996     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02346185     Document Type: Article

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