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Correction: A Nationwide Study of Norwegian Patients with Hereditary Angioedema with C1 Inhibitor Deficiency Identified Six Novel Mutations in SERPING1
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Public Library of Science
2015
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4536201/ https://www.ncbi.nlm.nih.gov/pubmed/26270546 http://dx.doi.org/10.1371/journal.pone.0136011 |
| _version_ | 1782385704306737152 |
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| author | Johnsrud, Irene Kulseth, Mari Ann Rødningen, Olaug Kristin Landrø, Linn Helsing, Per Waage Nielsen, Erik Heimdal, Ketil |
| author_facet | Johnsrud, Irene Kulseth, Mari Ann Rødningen, Olaug Kristin Landrø, Linn Helsing, Per Waage Nielsen, Erik Heimdal, Ketil |
| author_sort | Johnsrud, Irene |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-4536201 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2015 |
| publisher | Public Library of Science |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-45362012015-08-20 Correction: A Nationwide Study of Norwegian Patients with Hereditary Angioedema with C1 Inhibitor Deficiency Identified Six Novel Mutations in SERPING1 Johnsrud, Irene Kulseth, Mari Ann Rødningen, Olaug Kristin Landrø, Linn Helsing, Per Waage Nielsen, Erik Heimdal, Ketil PLoS One Correction Public Library of Science 2015-08-13 /pmc/articles/PMC4536201/ /pubmed/26270546 http://dx.doi.org/10.1371/journal.pone.0136011 Text en © 2015 Johnsrud 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
| spellingShingle | Correction Johnsrud, Irene Kulseth, Mari Ann Rødningen, Olaug Kristin Landrø, Linn Helsing, Per Waage Nielsen, Erik Heimdal, Ketil Correction: A Nationwide Study of Norwegian Patients with Hereditary Angioedema with C1 Inhibitor Deficiency Identified Six Novel Mutations in SERPING1 |
| title | Correction: A Nationwide Study of Norwegian Patients with Hereditary Angioedema with C1 Inhibitor Deficiency Identified Six Novel Mutations in SERPING1
|
| title_full | Correction: A Nationwide Study of Norwegian Patients with Hereditary Angioedema with C1 Inhibitor Deficiency Identified Six Novel Mutations in SERPING1
|
| title_fullStr | Correction: A Nationwide Study of Norwegian Patients with Hereditary Angioedema with C1 Inhibitor Deficiency Identified Six Novel Mutations in SERPING1
|
| title_full_unstemmed | Correction: A Nationwide Study of Norwegian Patients with Hereditary Angioedema with C1 Inhibitor Deficiency Identified Six Novel Mutations in SERPING1
|
| title_short | Correction: A Nationwide Study of Norwegian Patients with Hereditary Angioedema with C1 Inhibitor Deficiency Identified Six Novel Mutations in SERPING1
|
| title_sort | correction: a nationwide study of norwegian patients with hereditary angioedema with c1 inhibitor deficiency identified six novel mutations in serping1 |
| topic | Correction |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4536201/ https://www.ncbi.nlm.nih.gov/pubmed/26270546 http://dx.doi.org/10.1371/journal.pone.0136011 |
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