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Case Report: An Infant with Severe Thrombocytopenia Diagnosed with Type 2B von Willebrand Disease Due To a De Novo p.Val1316Met Mutation
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Galenos Publishing
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7702659/ https://www.ncbi.nlm.nih.gov/pubmed/32618441 http://dx.doi.org/10.4274/tjh.galenos.2020.2020.0213 |
| _version_ | 1783616588672401408 |
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| author | Fan, Junjie Ling, Jing Zhou, Huifeng He, Jie Hu, Shaoyan |
| author_facet | Fan, Junjie Ling, Jing Zhou, Huifeng He, Jie Hu, Shaoyan |
| author_sort | Fan, Junjie |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-7702659 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2020 |
| publisher | Galenos Publishing |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-77026592020-12-05 Case Report: An Infant with Severe Thrombocytopenia Diagnosed with Type 2B von Willebrand Disease Due To a De Novo p.Val1316Met Mutation Fan, Junjie Ling, Jing Zhou, Huifeng He, Jie Hu, Shaoyan Turk J Haematol Letters to the Editor Galenos Publishing 2020-12 2020-11-19 /pmc/articles/PMC7702659/ /pubmed/32618441 http://dx.doi.org/10.4274/tjh.galenos.2020.2020.0213 Text en © Copyright 2020 by Turkish Society of Hematology / Turkish Journal of Hematology, Published by Galenos Publishing House. http://creativecommons.org/licenses/by/2.5/ 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 work is properly cited. |
| spellingShingle | Letters to the Editor Fan, Junjie Ling, Jing Zhou, Huifeng He, Jie Hu, Shaoyan Case Report: An Infant with Severe Thrombocytopenia Diagnosed with Type 2B von Willebrand Disease Due To a De Novo p.Val1316Met Mutation |
| title | Case Report: An Infant with Severe Thrombocytopenia Diagnosed with Type 2B von Willebrand Disease Due To a De Novo p.Val1316Met Mutation |
| title_full | Case Report: An Infant with Severe Thrombocytopenia Diagnosed with Type 2B von Willebrand Disease Due To a De Novo p.Val1316Met Mutation |
| title_fullStr | Case Report: An Infant with Severe Thrombocytopenia Diagnosed with Type 2B von Willebrand Disease Due To a De Novo p.Val1316Met Mutation |
| title_full_unstemmed | Case Report: An Infant with Severe Thrombocytopenia Diagnosed with Type 2B von Willebrand Disease Due To a De Novo p.Val1316Met Mutation |
| title_short | Case Report: An Infant with Severe Thrombocytopenia Diagnosed with Type 2B von Willebrand Disease Due To a De Novo p.Val1316Met Mutation |
| title_sort | case report: an infant with severe thrombocytopenia diagnosed with type 2b von willebrand disease due to a de novo p.val1316met mutation |
| topic | Letters to the Editor |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7702659/ https://www.ncbi.nlm.nih.gov/pubmed/32618441 http://dx.doi.org/10.4274/tjh.galenos.2020.2020.0213 |
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