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Volumn 99, Issue 8, 2002, Pages 2670-2676
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Sustained phenotypic correction of hemophilia B dogs with a factor IX null mutation by liver-directed gene therapy
a,b a,b b a,b a,b a,b a,b a,b a,b a,b a,b
b
NONE
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Author keywords
[No Author keywords available]
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Indexed keywords
AAV (APOE)4 HAAT;
AAV (APOE)4 HAAT CFIX;
ADENOVIRUS VECTOR;
BLOOD CLOTTING FACTOR 9;
NEUTRALIZING ANTIBODY;
UNCLASSIFIED DRUG;
ANIMAL EXPERIMENT;
ANIMAL MODEL;
ARTICLE;
BLOOD CLOTTING TIME;
CONTROLLED STUDY;
DNA VECTOR;
DOSE RESPONSE;
GENE MUTATION;
GENE THERAPY;
GENE TRANSFER;
HEMOPHILIA B;
LIVER;
NONHUMAN;
PARTIAL THROMBOPLASTIN TIME;
PHENOTYPE;
PRIORITY JOURNAL;
TREATMENT OUTCOME;
VIRAL GENE DELIVERY SYSTEM;
X CHROMOSOME LINKAGE;
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EID: 0037089331
PISSN: 00064971
EISSN: None
Source Type: Journal
DOI: 10.1182/blood.V99.8.2670 Document Type: Article |
Times cited : (293)
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References (35)
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