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Article: NF‐E2 mutation as a novel cause for inherited thrombocytopenia

TitleNF‐E2 mutation as a novel cause for inherited thrombocytopenia
Authors
Luk, ADWYANG, XAlcasabas, APHao, RCChan, KWLee, PPYang, JChan, GCFSo, JCCYang, WLau, YL
Keywordsblood smear
bone marrow examination
case report
clinical article
Filipino (citizen)
Issue Date2020
PublisherWiley-Blackwell Publishing Ltd. The Journal's web site is located at http://www.blackwellpublishing.com/journals/BJH
Citation
British Journal of Haematology, 2020, v. 189, p. e31-e63 How to Cite?
DOI: http://dx.doi.org/10.1111/bjh.16438
Persistent Identifierhttp://hdl.handle.net/10722/289150
ISSN
0007-1048
2023 Impact Factor: 5.1
2023 SCImago Journal Rankings: 1.574
PubMed Central ID
PMC7187305
ISI Accession Number ID
WOS:000525306600004

 

DC FieldValueLanguage
dc.contributor.authorLuk, ADW-
dc.contributor.authorYANG, X-
dc.contributor.authorAlcasabas, AP-
dc.contributor.authorHao, RC-
dc.contributor.authorChan, KW-
dc.contributor.authorLee, PP-
dc.contributor.authorYang, J-
dc.contributor.authorChan, GCF-
dc.contributor.authorSo, JCC-
dc.contributor.authorYang, W-
dc.contributor.authorLau, YL-
dc.date.accessioned2020-10-22T08:08:31Z-
dc.date.available2020-10-22T08:08:31Z-
dc.date.issued2020-
dc.identifier.citationBritish Journal of Haematology, 2020, v. 189, p. e31-e63-
dc.identifier.issn0007-1048-
dc.identifier.urihttp://hdl.handle.net/10722/289150-
dc.languageeng-
dc.publisherWiley-Blackwell Publishing Ltd. The Journal's web site is located at http://www.blackwellpublishing.com/journals/BJH-
dc.relation.ispartofBritish Journal of Haematology-
dc.rightsPreprint This is the pre-peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. Postprint This is the peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectblood smear-
dc.subjectbone marrow examination-
dc.subjectcase report-
dc.subjectclinical article-
dc.subjectFilipino (citizen)-
dc.titleNF‐E2 mutation as a novel cause for inherited thrombocytopenia-
dc.typeArticle-
dc.identifier.emailChan, KW: kwchan@hku.hk-
dc.identifier.emailLee, PP: ppwlee@hku.hk-
dc.identifier.emailYang, J: jingy09@hku.hk-
dc.identifier.emailChan, GCF: gcfchan@hku.hk-
dc.identifier.emailYang, W: yangwl@hku.hk-
dc.identifier.emailLau, YL: lauylung@hku.hk-
dc.identifier.authorityLee, PP=rp00462-
dc.identifier.authorityChan, GCF=rp00431-
dc.identifier.authorityYang, W=rp00524-
dc.identifier.authorityLau, YL=rp00361-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1111/bjh.16438-
dc.identifier.pmid31951293-
dc.identifier.pmcidPMC7187305-
dc.identifier.scopuseid_2-s2.0-85078305359-
dc.identifier.hkuros316126-
dc.identifier.volume189-
dc.identifier.spagee31-
dc.identifier.epagee63-
dc.identifier.isiWOS:000525306600004-
dc.publisher.placeUnited Kingdom-
dc.identifier.issnl0007-1048-

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