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iText 4.2.0 by 1T3XT2019-07-12T12:46:57+05:30Arbortext Advanced Print Publisher2020-02-10T02:24:17-08:002020-02-10T02:24:17-08:00uuid:8addd02c-2a8d-4824-a074-0375b52bef83uuid:9735c38c-787b-4f5b-aca7-e8422204bc96JournalHemoglobin© 2019 Informa UK Limited, trading as Taylor & Francis Group0363-02691532-432X43277-82778210.1080/03630269.2019.1601107https://doi.org/10.1080/03630269.2019.1601107application/pdf10.1080/03630269.2019.1601107en-USA Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with β-Thalassemia Trait Results in Severe Hemolytic AnemiaTaylor & FrancisHemoglobin, 2019. doi: 10.1080/03630269.2019.1601107Klei Thomas R. L.Kheradmand Kia SimaVeldthuis MartijnDehbozorgian JavadKarimi MehranGeissler JudySellink EricaThiel-Valkhof MarijkeBurger Patrickvan Alphen FlorisMeijer Alexander B.van Bruggen Robinvan Zwieten Robα-Thalassemia (α-thal)anemiaβ-thalassemia (β-thal)erythrocyteHb Charlieuhemoglobin (Hb)VoR2019-06-13truewww.tandfonline.com10.1080/03630269.2019.1601107www.tandfonline.comtrue2019-06-1310.1080/03630269.2019.1601107
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