Potential limits of AAV‐based gene therapy with the use of new transgenes expressing factor IX fusion proteins.

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Title: Potential limits of AAV‐based gene therapy with the use of new transgenes expressing factor IX fusion proteins.
Authors: Le Quellec, Sandra1,2, Enjolras, Nathalie1,2, Negrier, Claude1,2, Dane, Allison3, McIntosh, Jenny3, Rosales, Cecilia3, Nathwani, Amit3
Source: Haemophilia. Jan2019, Vol. 25 Issue 1, pe11-e18. 8p. 3 Graphs.
Database: Academic Search Ultimate
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An: 134233276
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  Data: Potential limits of AAV‐based gene therapy with the use of new transgenes expressing factor IX fusion proteins.
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  Data: <searchLink fieldCode="JN" term="%22Haemophilia%22">Haemophilia</searchLink>. Jan2019, Vol. 25 Issue 1, pe11-e18. 8p. 3 Graphs.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=134233276
RecordInfo BibRecord:
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      – Type: doi
        Value: 10.1111/hae.13651
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      – Code: eng
        Text: English
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        PageCount: 8
        StartPage: e11
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      – TitleFull: Potential limits of AAV‐based gene therapy with the use of new transgenes expressing factor IX fusion proteins.
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            NameFull: Le Quellec, Sandra
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            NameFull: Enjolras, Nathalie
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            NameFull: Negrier, Claude
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            NameFull: Dane, Allison
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            NameFull: McIntosh, Jenny
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            NameFull: Rosales, Cecilia
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            – D: 01
              M: 01
              Text: Jan2019
              Type: published
              Y: 2019
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