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The First Korean Hemoglobinopathy With Unique Hemoglobin Electrophoresis Results Diagnosed as Hemoglobin Boras.

作者信息

Bae Jeongyun, Ahn Won Kee, Jang Jaehyeok, Jang Hanmil, Kang Hyein, Rim John Hoon, Hahn Seung Min, Han Jung Woo, Lyu Chuhl Joo, Lim Jong-Baeck

机构信息

Department of Laboratory Medicine, Yonsei University College of Medicine, Seoul, Korea.

Division of Pediatric Hematology and Oncology, Department of Pediatrics, Yonsei University College of Medicine, Seoul, Korea.

出版信息

Ann Lab Med. 2024 Jan 1;44(1):97-99. doi: 10.3343/alm.2024.44.1.97. Epub 2023 Sep 4.

DOI:10.3343/alm.2024.44.1.97
PMID:37665291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10485859/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7520/10485859/1b6cd987cc22/alm-44-1-97-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7520/10485859/1b6cd987cc22/alm-44-1-97-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7520/10485859/1b6cd987cc22/alm-44-1-97-f1.jpg

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本文引用的文献

1
Unstable hemoglobin Montreal II uncovered in an adult with unexplained hemolysis exacerbated by a presumed viral infection: a case report.不稳定血红蛋白蒙特利尔 II 型在不明原因溶血性贫血的成人中被发现,该贫血由疑似病毒感染加重:病例报告。
J Med Case Rep. 2022 Apr 10;16(1):145. doi: 10.1186/s13256-022-03374-y.
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Analysis of a Novel Mexican Variant of the Gene Associated with β-Thalassemia Using Bioinformatic Tools.使用生物信息学工具分析与β地中海贫血相关基因的一种新型墨西哥变体。
Hemoglobin. 2021 Mar;45(2):87-93. doi: 10.1080/03630269.2021.1920976. Epub 2021 Jun 1.
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Updates of the HbVar database of human hemoglobin variants and thalassemia mutations.
人类血红蛋白变异体和地中海贫血突变的 HbVar 数据库更新。
Nucleic Acids Res. 2014 Jan;42(Database issue):D1063-9. doi: 10.1093/nar/gkt911. Epub 2013 Oct 16.
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The diagnostic dilemma of congenital unstable hemoglobinopathies.先天性不稳定血红蛋白病的诊断困境。
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Evaluation of anemia in children.儿童贫血评估。
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The unstable haemoglobins.不稳定血红蛋白
Blood Rev. 1993 Sep;7(3):146-63. doi: 10.1016/0268-960x(93)90002-l.
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New unstable haemoglobin borås: beta 88 (F4) leucine-arginine.
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Hb Borås or alpha 2 beta 2(88)(F4)Leu----Arg in a South African female.
Hemoglobin. 1987;11(2):157-60. doi: 10.3109/03630268709005791.