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filingDate 2013-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2019-09-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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publicationDate 2019-09-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-10398787-B2
titleOfInvention Vectors for liver-directed gene therapy of hemophilia and methods and use thereof
abstract The present invention relates to vectors containing liver-specific regulatory sequences and codon-optimized factor IX or factor VIII genes, methods employing these vectors and uses of these vectors. Expression cassettes and vectors containing these liver-specific regulatory elements and codon-optimized factor IX or factor VIII genes are also disclosed. The present invention is particularly useful for applications using gene therapy, in particular for the treatment of hemophilia A and B.
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priorityDate 2012-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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