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Volumn 277, Issue 2, 2002, Pages 1375-1380
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Biochemical analysis of a missense mutation in aceruloplasminemia
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Author keywords
[No Author keywords available]
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Indexed keywords
MOLECULAR PATHOGENESIS;
BIOSYNTHESIS;
DISEASES;
DNA;
GENES;
MUTAGENESIS;
NEUROLOGY;
BIOCHEMISTRY;
ARGININE;
BLOOD CLOTTING FACTOR 8;
CERULOPLASMIN;
COMPLEMENTARY DNA;
COPPER 64;
GLYCOSYLPHOSPHATIDYLINOSITOL;
HEPHAESTIN;
PROTEIN DERIVATIVE;
UNCLASSIFIED DRUG;
ACERULOPLASMINEMIA;
ANIMAL CELL;
ARTICLE;
BIOCHEMISTRY;
CELL LABELING;
CHO CELL;
CONTROLLED STUDY;
DEGENERATIVE DISEASE;
ENDOPLASMIC RETICULUM;
GENETIC CONSERVATION;
GENETIC TRANSFECTION;
GLYCOSYLATION;
HUMAN;
HUMAN CELL;
MISSENSE MUTATION;
NONHUMAN;
PATHOGENESIS;
PRIORITY JOURNAL;
PROTEIN SECRETION;
AMINO ACID SEQUENCE;
ANIMALS;
CERULOPLASMIN;
CHO CELLS;
COPPER;
CRICETINAE;
GLYCOSYLPHOSPHATIDYLINOSITOLS;
HUMANS;
IMMUNOHISTOCHEMISTRY;
IRON;
MOLECULAR SEQUENCE DATA;
MOLECULAR STRUCTURE;
MUTAGENESIS, SITE-DIRECTED;
MUTATION, MISSENSE;
NEURODEGENERATIVE DISEASES;
ANIMALIA;
CRICETINAE;
CRICETULUS GRISEUS;
MAMMALIA;
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EID: 0037059741
PISSN: 00219258
EISSN: None
Source Type: Journal
DOI: 10.1074/jbc.M109123200 Document Type: Article |
Times cited : (78)
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References (36)
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