A factor IX-deficient mouse model for hemophilia B gene therapy

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

Volumn 94, Issue 21, 1997, Pages 11563-11566

  Wang, L ^a   Zoppe, M ^a   Hackeng, T M ^a   Griffin, J H ^a   Lee, K F ^a   Verma, I M ^a  

^a SALK INSTITUTE FOR BIOLOGICAL STUDIES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 9;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BLEEDING DISORDER; BLOOD CLOTTING; CONTROLLED STUDY; GENE DISRUPTION; GENE THERAPY; HEMOPHILIA B; MOUSE; NONHUMAN; PARTIAL THROMBOPLASTIN TIME; PRIORITY JOURNAL; RECOMBINANT GENE; VIRUS RECOMBINANT;

ADENOVIRIDAE; ANIMALS; EXONS; FACTOR IX; FEMALE; GENE THERAPY; GENE TRANSFER TECHNIQUES; GENETIC VECTORS; GENOMIC LIBRARY; HEMOPHILIA B; HETEROZYGOTE; HOMOZYGOTE; HUMANS; MALE; MICE; MICE, INBRED C57BL; MICE, INBRED STRAINS; MICE, KNOCKOUT; RECOMBINATION, GENETIC;

EID: 0030758328     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.94.21.11563     Document Type: Article

References (23)