|
Volumn 355, Issue 6363, 1992, Pages 836-838
|
Defective anion transport activity of the abnormal band 3 in hereditary ovalocytic red blood cells
|
Author keywords
[No Author keywords available]
|
Indexed keywords
ERYTHROCYTE BAND 3 PROTEIN;
AMINO ACID;
COMPLEMENTARY DNA;
ANION TRANSPORT;
ARTICLE;
ELLIPTOCYTOSIS;
ERYTHROCYTE;
HUMAN;
HUMAN CELL;
PRIORITY JOURNAL;
AMINO TERMINAL SEQUENCE;
CYTOPLASM;
ERYTHROCYTE DISORDER;
ERYTHROID CELL;
GENE DELETION;
HEREDITARY OVALOCYTOSIS;
MALARIA;
OVALOCYTIC RED BLOOD CELL;
PARASITEMIA;
PLASMODIUM FALCIPARUM;
POINT MUTATION;
POLYACRYLAMIDE GEL ELECTROPHORESIS;
POLYMERASE CHAIN REACTION;
PROTEIN STRUCTURE;
SOUTHEAST ASIAN;
4,4'-DIISOTHIOCYANOSTILBENE-2,2'-DISULFONIC ACID;
4-ACETAMIDO-4'-ISOTHIOCYANATOSTILBENE-2,2'-DISULFONIC ACID;
AMINO ACID SEQUENCE;
ANION EXCHANGE PROTEIN 1, ERYTHROCYTE;
BINDING SITES;
CHROMOSOME DELETION;
ELLIPTOCYTOSIS, HEREDITARY;
ERYTHROCYTES;
HUMAN;
KINETICS;
MOLECULAR SEQUENCE DATA;
MUTATION;
REFERENCE VALUES;
SULFATES;
SUPPORT, NON-U.S. GOV'T;
|
EID: 0026584441
PISSN: 00280836
EISSN: None
Source Type: Journal
DOI: 10.1038/355836a0 Document Type: Article |
Times cited : (148)
|
References (21)
|