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Familial Hemophagocytic Lymphohistiocytosis Type 2 in a Korean Infant With Compound Heterozygous PRF1 Defects Involving a PRF1 Mutation, c.1091T>G
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
The Korean Society for Laboratory Medicine
2017
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5203996/ https://www.ncbi.nlm.nih.gov/pubmed/28029005 http://dx.doi.org/10.3343/alm.2017.37.2.162 |
| _version_ | 1782489821771464704 |
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| author | Kim, Min-Sun Cho, Young-Uk Jang, Seongsoo Seo, Eul-Ju Im, Ho Joon Park, Chan-Jeoung |
| author_facet | Kim, Min-Sun Cho, Young-Uk Jang, Seongsoo Seo, Eul-Ju Im, Ho Joon Park, Chan-Jeoung |
| author_sort | Kim, Min-Sun |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-5203996 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2017 |
| publisher | The Korean Society for Laboratory Medicine |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-52039962017-03-01 Familial Hemophagocytic Lymphohistiocytosis Type 2 in a Korean Infant With Compound Heterozygous PRF1 Defects Involving a PRF1 Mutation, c.1091T>G Kim, Min-Sun Cho, Young-Uk Jang, Seongsoo Seo, Eul-Ju Im, Ho Joon Park, Chan-Jeoung Ann Lab Med Letter to the Editor The Korean Society for Laboratory Medicine 2017-03 2016-12-20 /pmc/articles/PMC5203996/ /pubmed/28029005 http://dx.doi.org/10.3343/alm.2017.37.2.162 Text en © The Korean Society for Laboratory Medicine. http://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 (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
| spellingShingle | Letter to the Editor Kim, Min-Sun Cho, Young-Uk Jang, Seongsoo Seo, Eul-Ju Im, Ho Joon Park, Chan-Jeoung Familial Hemophagocytic Lymphohistiocytosis Type 2 in a Korean Infant With Compound Heterozygous PRF1 Defects Involving a PRF1 Mutation, c.1091T>G |
| title | Familial Hemophagocytic Lymphohistiocytosis Type 2 in a Korean Infant With Compound Heterozygous PRF1 Defects Involving a PRF1 Mutation, c.1091T>G |
| title_full | Familial Hemophagocytic Lymphohistiocytosis Type 2 in a Korean Infant With Compound Heterozygous PRF1 Defects Involving a PRF1 Mutation, c.1091T>G |
| title_fullStr | Familial Hemophagocytic Lymphohistiocytosis Type 2 in a Korean Infant With Compound Heterozygous PRF1 Defects Involving a PRF1 Mutation, c.1091T>G |
| title_full_unstemmed | Familial Hemophagocytic Lymphohistiocytosis Type 2 in a Korean Infant With Compound Heterozygous PRF1 Defects Involving a PRF1 Mutation, c.1091T>G |
| title_short | Familial Hemophagocytic Lymphohistiocytosis Type 2 in a Korean Infant With Compound Heterozygous PRF1 Defects Involving a PRF1 Mutation, c.1091T>G |
| title_sort | familial hemophagocytic lymphohistiocytosis type 2 in a korean infant with compound heterozygous prf1 defects involving a prf1 mutation, c.1091t>g |
| topic | Letter to the Editor |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5203996/ https://www.ncbi.nlm.nih.gov/pubmed/28029005 http://dx.doi.org/10.3343/alm.2017.37.2.162 |
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