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Mutations in the gene encoding the PML nuclear body protein Sp110 are associated with immunodeficiency and hepatic veno-occlusive disease.

Mutations in the gene encoding the PML nuclear body protein Sp110 are associated with immunodeficiency and hepatic veno-occlusive disease.
Mutations in the gene encoding the PML nuclear body protein Sp110 are associated with immunodeficiency and hepatic veno-occlusive disease.
We describe mutations in the PML nuclear body protein Sp110 in the syndrome veno-occlusive disease with immunodeficiency, an autosomal recessive disorder of severe hypogammaglobulinemia, combined T and B cell immunodeficiency, absent lymph node germinal centers, absent tissue plasma cells and hepatic veno-occlusive disease. This is the first report of the involvement of a nuclear body protein in a human primary immunodeficiency and of high-penetrance genetic mutations in hepatic veno-occlusive disease.
1061-4036
620-622
Roscioli, Tony
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Cliffe, Simon T.
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Bloch, Donald B.
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Bell, Christopher G.
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Mullan, Glenda
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Taylor, Peter J.
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Sarris, Maria
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Wang, Joanne
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Donald, Jennifer A.
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Kirk, Edwin P.
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Ziegler, John B.
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Salzer, Ulrich
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McDonald, George B.
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Wong, Melanie
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Lindeman, Robert
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Buckley, Michael F.
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Roscioli, Tony
35e31db3-11fd-4adf-96c6-6014f7bd9838
Cliffe, Simon T.
061a343b-eab7-48d3-b3d5-9e2bc854ac3d
Bloch, Donald B.
bce63551-89d0-4ccc-b03a-4a2a5278eaf7
Bell, Christopher G.
44982df7-0746-4cdb-bed1-0bdfe68f1a64
Mullan, Glenda
ac01e624-d401-4d56-9b2a-dc7322084146
Taylor, Peter J.
01694c3d-180d-41d2-80e0-c7d892e3f3f6
Sarris, Maria
c8b919ff-c536-479d-89e1-876f69d3b826
Wang, Joanne
6eedb4d6-ca98-4e44-96bc-a9c5e915e751
Donald, Jennifer A.
208832be-5f04-42fa-be52-36cacc0dc2bb
Kirk, Edwin P.
ace0fc4d-4165-42c2-b521-8539ead1c8a0
Ziegler, John B.
626d5f03-fded-4294-b00e-ea68f2eed23f
Salzer, Ulrich
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McDonald, George B.
de3d0397-6ba1-4d6a-a354-3c7a3f1e3170
Wong, Melanie
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Lindeman, Robert
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Buckley, Michael F.
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Roscioli, Tony, Cliffe, Simon T., Bloch, Donald B., Bell, Christopher G., Mullan, Glenda, Taylor, Peter J., Sarris, Maria, Wang, Joanne, Donald, Jennifer A., Kirk, Edwin P., Ziegler, John B., Salzer, Ulrich, McDonald, George B., Wong, Melanie, Lindeman, Robert and Buckley, Michael F. (2006) Mutations in the gene encoding the PML nuclear body protein Sp110 are associated with immunodeficiency and hepatic veno-occlusive disease. Nature Genetics, 38 (6), 620-622. (doi:10.1038/ng1780). (PMID:16648851)

Record type: Article

Abstract

We describe mutations in the PML nuclear body protein Sp110 in the syndrome veno-occlusive disease with immunodeficiency, an autosomal recessive disorder of severe hypogammaglobulinemia, combined T and B cell immunodeficiency, absent lymph node germinal centers, absent tissue plasma cells and hepatic veno-occlusive disease. This is the first report of the involvement of a nuclear body protein in a human primary immunodeficiency and of high-penetrance genetic mutations in hepatic veno-occlusive disease.

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Accepted/In Press date: 14 March 2006
e-pub ahead of print date: 30 April 2006
Published date: June 2006
Organisations: Human Development & Health, Centre for Biological Sciences, MRC Life-Course Epidemiology Unit

Identifiers

Local EPrints ID: 400997
URI: http://eprints.soton.ac.uk/id/eprint/400997
ISSN: 1061-4036
PURE UUID: c9df162a-19d7-42b4-bc70-5b9a2226d086
ORCID for Christopher G. Bell: ORCID iD orcid.org/0000-0003-4601-1242

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Date deposited: 03 Oct 2016 13:48
Last modified: 15 Mar 2024 02:36

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Contributors

Author: Tony Roscioli
Author: Simon T. Cliffe
Author: Donald B. Bloch
Author: Christopher G. Bell ORCID iD
Author: Glenda Mullan
Author: Peter J. Taylor
Author: Maria Sarris
Author: Joanne Wang
Author: Jennifer A. Donald
Author: Edwin P. Kirk
Author: John B. Ziegler
Author: Ulrich Salzer
Author: George B. McDonald
Author: Melanie Wong
Author: Robert Lindeman
Author: Michael F. Buckley

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