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Enhancing transduction of the liver by adeno-associated viral vectors

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Year: 2008
Type: article
Source: Gene Therapy
DOI: 10.1038/gt.2008.137
Authors: A C Nathwani, M Cochrane, J McIntosh, C Y C Ng, J Zhou, J T Gray, A M Davidoff
Institutions: University College London, St. Jude Children's Research Hospital
Language: English

Topic: Virus-based gene therapy research
Subfield: Genetics
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: green

Funders: American Lebanese Syrian Associated Charities, National Institute for Health and Care Research, University College London Hospitals NHS Foundation Trust, National Heart, Lung, and Blood Institute
Awards: Clinical trial of self complementary AAV8-mediated gene transfer for hemophilia B, AAV-Mediated Gene Therapy for Hemophilia
OpenAlex ID: W2084114153
FWCI: 3.043
Cites: 41
Cited by: 77
Related to: 10
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