Inherited or de novo mutation affecting aspartate 18 of TREX1 results in either familial chilblain lupus or Aicardi-Goutières syndrome
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| Veröffentlicht in: | The British journal of dermatology 2012, Vol.167 (1), p.212-214 |
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| Format: | Report |
| Sprache: | eng |
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| container_end_page | 214 |
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| container_issue | 1 |
| container_start_page | 212 |
| container_title | The British journal of dermatology |
| container_volume | 167 |
| creator | Tüngler, V Silver, R M Walkenhorst, H Günther, C Lee-Kirsch, M A |
| description | |
| doi_str_mv | 10.1111/j.1365-2133.2012.10813.x |
| format | Report |
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| fulltext | fulltext |
| identifier | EISSN: 1365-2133 |
| ispartof | The British journal of dermatology, 2012, Vol.167 (1), p.212-214 |
| issn | 1365-2133 |
| language | eng |
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| source | Oxford University Press Journals All Titles (1996-Current); Wiley Online Library All Journals |
| title | Inherited or de novo mutation affecting aspartate 18 of TREX1 results in either familial chilblain lupus or Aicardi-Goutières syndrome |
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