Monosomy 1p36 is a subtelomeric deletion syndrome associated with congenital anomalies presumably due to haploinsufficiency of multiple genes. Although immunodeficiency has not been reported, genes encoding costimulatory molecules of the TNF receptor superfamily (TNFRSF) are within 1p36 and may be a...
Bibliographische Detailangaben
| Veröffentlicht in: | Clinical immunology (Orlando, Fla.). - 1999. - 128(2008), 2 vom: 15. Aug., Seite 181-9
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| 1. Verfasser: |
Suhoski, M M
(VerfasserIn) |
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| Weitere Verfasser: |
Perez, E E,
Heltzer, M L,
Laney, A,
Shaffer, L G,
Saitta, S,
Nachman, S,
Spinner, N B,
June, C H,
Orange, J S |
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| Format: | Online-Aufsatz
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| Sprache: | English |
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| Veröffentlicht: |
2008
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| Zugriff auf das übergeordnete Werk: | Clinical immunology (Orlando, Fla.)
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| Schlagworte: | Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Receptors, OX40 |
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