Functional expression of the Wilson disease protein reveals mislocalization and impaired copper-dependent trafficking of the common H1069Q mutation

Proceedings of the National Academy of Sciences of the United States of America

Volumn 95, Issue 18, 1998, Pages 10854-10859

  Payne, Aimee S ^a   Kelly, Edward J ^b   Gitlin, Jonathan D ^a,c  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF WASHINGTON   (United States)

^c ST LOUIS CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN; UNCLASSIFIED DRUG; WILSON PROTEIN;

ARTICLE; COPPER METABOLISM; ENDOPLASMIC RETICULUM; MUTATION; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; PROTEIN TRANSPORT; WILSON DISEASE;

ADENOSINE TRIPHOSPHATASES; ANIMALS; CARRIER PROTEINS; CATION TRANSPORT PROTEINS; CLONING, MOLECULAR; COPPER; DNA, COMPLEMENTARY; MICE; MUTAGENESIS, SITE-DIRECTED; MUTATION; PROTEIN FOLDING;

MAMMALIA;

EID: 0032167856     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.95.18.10854     Document Type: Article

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