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Sa.76. Ipex Syndrome with Normal FOXP3 Coding Region Sequences But Diminished FOXP3 Transcription and Translation: An Implied FOXP3 Regulatory Gene Defect

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Title: Sa.76. Ipex Syndrome with Normal FOXP3 Coding Region Sequences But Diminished FOXP3 Transcription and Translation: An Implied FOXP3 Regulatory Gene Defect
Authors: Schaffer, Frederick1, Cochran, Joe1, Key, L.1, Chatila, Talal2, Anover, S.3, Hackett, M.3, Ochs, Hans3, Torgerson, Troy3
Source: Clinical Immunology. Apr2006 Supplement 1, Vol. 119, pS131-S132. 0p.
Database: Academic Search Ultimate
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DbLabel: Academic Search Ultimate
An: 20883953
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
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  Data: Sa.76. Ipex Syndrome with Normal FOXP3 Coding Region Sequences But Diminished FOXP3 Transcription and Translation: An Implied FOXP3 Regulatory Gene Defect
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  Data: <searchLink fieldCode="JN" term="%22Clinical+Immunology%22">Clinical Immunology</searchLink>. Apr2006 Supplement 1, Vol. 119, pS131-S132. 0p.
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      – Type: doi
        Value: 10.1016/j.clim.2006.04.308
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      – Code: eng
        Text: English
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        StartPage: S131
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      – TitleFull: Sa.76. Ipex Syndrome with Normal FOXP3 Coding Region Sequences But Diminished FOXP3 Transcription and Translation: An Implied FOXP3 Regulatory Gene Defect
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            NameFull: Schaffer, Frederick
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            NameFull: Chatila, Talal
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            NameFull: Anover, S.
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            – D: 02
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              Text: Apr2006 Supplement 1
              Type: published
              Y: 2006
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              Value: 119
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            – TitleFull: Clinical Immunology
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