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filingDate 2022-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d541d5448afbaf0bda114a66543b48d3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8638ccaf899de727801917d6588c3848
publicationDate 2023-01-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2023022390-A1
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.
priorityDate 2012-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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