تقرير
NF-E2 mutation as a novel cause for inherited thrombocytopenia.
| العنوان: | NF-E2 mutation as a novel cause for inherited thrombocytopenia. |
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| المؤلفون: | Luk ADW; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China., Yang X; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China., Alcasabas AP; Section of Pediatric Hematology-Oncology, University of the Philippines - Philippine General Hospital, Manila, Philippines., Hao RC; Section of Allergy and Immunology, University of the Philippines - Philippine General Hospital, Manila, Philippines., Chan KW; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China., Lee PP; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China.; The Hong Kong Children's Hospital, Hong Kong, China., Yang J; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China., Chan GC; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China.; The Hong Kong Children's Hospital, Hong Kong, China., So JC; The Hong Kong Children's Hospital, Hong Kong, China., Yang W; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China., Lau YL; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China.; The Hong Kong Children's Hospital, Hong Kong, China. |
| المصدر: | British journal of haematology [Br J Haematol] 2020 Apr; Vol. 189 (2), pp. e41-e44. Date of Electronic Publication: 2020 Jan 17. |
| نوع المنشور: | Case Reports; Letter |
| اللغة: | English |
| بيانات الدورية: | Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 0372544 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1365-2141 (Electronic) Linking ISSN: 00071048 NLM ISO Abbreviation: Br J Haematol Subsets: MEDLINE |
| أسماء مطبوعة: | Publication: Oxford : Wiley-Blackwell Original Publication: Oxford : Blackwell Scientific Publications |
| مواضيع طبية MeSH: | NF-E2 Transcription Factor, p45 Subunit/*adverse effects , Thrombocytopenia/*genetics, Humans ; Infant, Newborn ; Male ; Mutation |
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| المشرفين على المادة: | 0 (NF-E2 Transcription Factor, p45 Subunit) |
| تواريخ الأحداث: | Date Created: 20200118 Date Completed: 20201204 Latest Revision: 20201214 |
| رمز التحديث: | 20221213 |
| مُعرف محوري في PubMed: | PMC7187305 |
| DOI: | 10.1111/bjh.16438 |
| PMID: | 31951293 |
| قاعدة البيانات: | MEDLINE |
Full Text Finder | تدمد: | 1365-2141 |
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| DOI: | 10.1111/bjh.16438 |