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Volumn 275, Issue 36, 2000, Pages 27933-27939

Torsin A and its torsion dystonia-associated mutant forms are lumenal glycoproteins that exhibit distinct subcellular localizations

(3) Kustedjo, Karen a Bracey, Michael H a Cravatt, Benjamin F a

a SCRIPPS RESEARCH INSTITUTE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHAPERONE; GLUTAMIC ACID; GLYCOPROTEIN; PROTEIN TORSIN A; PROTEINASE; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; AUTOSOMAL DOMINANT DISORDER; GENE DELETION; HUMAN; HUMAN CELL; IMMUNOREACTIVITY; NONHUMAN; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN FOLDING; PROTEIN LOCALIZATION; SEQUENCE HOMOLOGY; TORSION DYSTONIA;

ANIMALS; CARRIER PROTEINS; CELL LINE; CELL NUCLEUS; COS CELLS; DYSTONIA MUSCULORUM DEFORMANS; HUMANS; MOLECULAR CHAPERONES; MUTAGENESIS, SITE-DIRECTED; RECOMBINANT PROTEINS; SEQUENCE DELETION; TRANSFECTION;

ANIMALIA; MAMMALIA;

EID: 0034623158 PISSN: 00219258 EISSN: None Source Type: Journal
DOI: 10.1074/jbc.M910025199 Document Type: Article

Times cited : (158)

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