Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis

Blood

Volumn 97, Issue 2, 2001, Pages 543-550

  Wandersee, Nancy J ^b   Roesch, Amanda N ^b   Hamblen, Nancy R ^b   De Moes, Joost ^a   Van Der Valk, Martin A ^b   Bronson, Roderick T ^b   Gimm, J Aura ^b   Mohandas, Narla ^b   Demant, Peter ^b   Barker, Jane E ^a  

^a JACKSON LABORATORY   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

DIMER; FODRIN; SPECTRIN; TETRAMER;

AMINO ACID SEQUENCE; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CYTOSKELETON; DELETION MUTANT; DIMERIZATION; ELLIPTOCYTOSIS; ERYTHROCYTE STRUCTURE; EXON; GENE INSERTION; HISTOPATHOLOGY; INTRON; MOUSE; MOUSE MUTANT; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; THROMBOSIS;

EID: 0035863842     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.V97.2.543     Document Type: Article

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