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Primary Sjögren's syndrome and high type I interferon signalling in a kindred with C2 deficiency
| Autores principales: | , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8969662/ https://www.ncbi.nlm.nih.gov/pubmed/35368972 http://dx.doi.org/10.1093/rap/rkac018 |
| _version_ | 1784679302838616064 |
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| author | Willemsen, Mathijs Van Nieuwenhove, Erika Seyed Tabib, Nasim Sadat Staels, Frederik Schrijvers, Rik De Somer, Lien Liston, Adrian Humblet-Baron, Stephanie Wouters, Carine |
| author_facet | Willemsen, Mathijs Van Nieuwenhove, Erika Seyed Tabib, Nasim Sadat Staels, Frederik Schrijvers, Rik De Somer, Lien Liston, Adrian Humblet-Baron, Stephanie Wouters, Carine |
| author_sort | Willemsen, Mathijs |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-8969662 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2022 |
| publisher | Oxford University Press |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-89696622022-04-01 Primary Sjögren's syndrome and high type I interferon signalling in a kindred with C2 deficiency Willemsen, Mathijs Van Nieuwenhove, Erika Seyed Tabib, Nasim Sadat Staels, Frederik Schrijvers, Rik De Somer, Lien Liston, Adrian Humblet-Baron, Stephanie Wouters, Carine Rheumatol Adv Pract Letter to the Editor (Case report) Oxford University Press 2022-03-21 /pmc/articles/PMC8969662/ /pubmed/35368972 http://dx.doi.org/10.1093/rap/rkac018 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the British Society for Rheumatology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
| spellingShingle | Letter to the Editor (Case report) Willemsen, Mathijs Van Nieuwenhove, Erika Seyed Tabib, Nasim Sadat Staels, Frederik Schrijvers, Rik De Somer, Lien Liston, Adrian Humblet-Baron, Stephanie Wouters, Carine Primary Sjögren's syndrome and high type I interferon signalling in a kindred with C2 deficiency |
| title | Primary Sjögren's syndrome and high type I interferon signalling in a kindred with C2 deficiency |
| title_full | Primary Sjögren's syndrome and high type I interferon signalling in a kindred with C2 deficiency |
| title_fullStr | Primary Sjögren's syndrome and high type I interferon signalling in a kindred with C2 deficiency |
| title_full_unstemmed | Primary Sjögren's syndrome and high type I interferon signalling in a kindred with C2 deficiency |
| title_short | Primary Sjögren's syndrome and high type I interferon signalling in a kindred with C2 deficiency |
| title_sort | primary sjögren's syndrome and high type i interferon signalling in a kindred with c2 deficiency |
| topic | Letter to the Editor (Case report) |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8969662/ https://www.ncbi.nlm.nih.gov/pubmed/35368972 http://dx.doi.org/10.1093/rap/rkac018 |
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