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Article: Novel point mutation of the α2-globin gene (HBA2) and a rare 2.4 kb deletion of the α1-globin gene (HBA1), identified in two chinese patients with Hb H disease

TitleNovel point mutation of the α2-globin gene (HBA2) and a rare 2.4 kb deletion of the α1-globin gene (HBA1), identified in two chinese patients with Hb H disease
Authors
Issue Date2014
PublisherInforma Healthcare. The Journal's web site is located at http://www.tandf.co.uk/journals/titles/03630269.asp
Citation
Hemoglobin, 2014, v. 38 n. 3, p. 213-215 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/201053
ISSN
2015 Impact Factor: 0.747
2015 SCImago Journal Rankings: 0.389
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorSo, JCCen_US
dc.contributor.authorChan, AYYen_US
dc.contributor.authorMa, ESKen_US
dc.date.accessioned2014-08-21T07:11:57Z-
dc.date.available2014-08-21T07:11:57Z-
dc.date.issued2014en_US
dc.identifier.citationHemoglobin, 2014, v. 38 n. 3, p. 213-215en_US
dc.identifier.issn0363-0269-
dc.identifier.urihttp://hdl.handle.net/10722/201053-
dc.languageengen_US
dc.publisherInforma Healthcare. The Journal's web site is located at http://www.tandf.co.uk/journals/titles/03630269.asp-
dc.relation.ispartofHemoglobinen_US
dc.rightsHemoglobin. Copyright © Informa Healthcare.-
dc.rightsCreative Commons: Attribution 3.0 Hong Kong License-
dc.titleNovel point mutation of the α2-globin gene (HBA2) and a rare 2.4 kb deletion of the α1-globin gene (HBA1), identified in two chinese patients with Hb H diseaseen_US
dc.typeArticleen_US
dc.identifier.emailSo, JCC: scc@pathology.hku.hken_US
dc.identifier.emailMa, ESK: eskma@HKUCC.hku.hk-
dc.identifier.authoritySo, JCC=rp00391en_US
dc.description.naturepostprint-
dc.identifier.doi10.3109/03630269.2014.894478en_US
dc.identifier.pmid24826793-
dc.identifier.hkuros231993en_US
dc.identifier.volume38en_US
dc.identifier.issue3en_US
dc.identifier.spage213en_US
dc.identifier.epage215en_US
dc.identifier.isiWOS:000336501500013-
dc.publisher.placeUnited Kingdom-

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