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A dominantly-inherited Behcet-like disorder caused by haploinsufficiency of the TNFAIP3/A20 protein
| Autores principales: | , , , , , , , , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2015
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4597176/ http://dx.doi.org/10.1186/1546-0096-13-S1-O71 |
| _version_ | 1782393877906325504 |
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| author | Zhou, Q Wang, H Chae, J Yang, D Demirkaya, E Stoffels, M Takeuchi, M Chen, C Ombrello, A Schwartz, D Hoffmann, P Stone, D Laxer, R Royen-Kerkhof, AV Ozen, S Gadina, M Kastner, D Aksentijevich, I |
| author_facet | Zhou, Q Wang, H Chae, J Yang, D Demirkaya, E Stoffels, M Takeuchi, M Chen, C Ombrello, A Schwartz, D Hoffmann, P Stone, D Laxer, R Royen-Kerkhof, AV Ozen, S Gadina, M Kastner, D Aksentijevich, I |
| author_sort | Zhou, Q |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-4597176 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2015 |
| publisher | BioMed Central |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-45971762015-10-08 A dominantly-inherited Behcet-like disorder caused by haploinsufficiency of the TNFAIP3/A20 protein Zhou, Q Wang, H Chae, J Yang, D Demirkaya, E Stoffels, M Takeuchi, M Chen, C Ombrello, A Schwartz, D Hoffmann, P Stone, D Laxer, R Royen-Kerkhof, AV Ozen, S Gadina, M Kastner, D Aksentijevich, I Pediatr Rheumatol Online J Oral Presentation BioMed Central 2015-09-28 /pmc/articles/PMC4597176/ http://dx.doi.org/10.1186/1546-0096-13-S1-O71 Text en Copyright © 2015 Zhou et al. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
| spellingShingle | Oral Presentation Zhou, Q Wang, H Chae, J Yang, D Demirkaya, E Stoffels, M Takeuchi, M Chen, C Ombrello, A Schwartz, D Hoffmann, P Stone, D Laxer, R Royen-Kerkhof, AV Ozen, S Gadina, M Kastner, D Aksentijevich, I A dominantly-inherited Behcet-like disorder caused by haploinsufficiency of the TNFAIP3/A20 protein |
| title | A dominantly-inherited Behcet-like disorder caused by haploinsufficiency of the TNFAIP3/A20 protein |
| title_full | A dominantly-inherited Behcet-like disorder caused by haploinsufficiency of the TNFAIP3/A20 protein |
| title_fullStr | A dominantly-inherited Behcet-like disorder caused by haploinsufficiency of the TNFAIP3/A20 protein |
| title_full_unstemmed | A dominantly-inherited Behcet-like disorder caused by haploinsufficiency of the TNFAIP3/A20 protein |
| title_short | A dominantly-inherited Behcet-like disorder caused by haploinsufficiency of the TNFAIP3/A20 protein |
| title_sort | dominantly-inherited behcet-like disorder caused by haploinsufficiency of the tnfaip3/a20 protein |
| topic | Oral Presentation |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4597176/ http://dx.doi.org/10.1186/1546-0096-13-S1-O71 |
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