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Hb Extremadura [β64(E8)Gly→Ser;β133(H11)Val→Leu]: a new molecular analysis.

作者信息

Ropero Paloma, Martín-Nuñez Guillermo, González F A, Villegas Ana, de la Fuente-Gonzalo Félix, Martínez-Nieto Jorge, Vinuesa Lara, Díaz-Mediavilla Joaquín

机构信息

Hematology Service, Hospital Clínico San Carlos, Madrid, Spain.

出版信息

Hemoglobin. 2011;35(4):423-7. doi: 10.3109/03630269.2011.576353.

DOI:10.3109/03630269.2011.576353
PMID:21797709
Abstract

Unstable hemoglobin (Hb) variants account for 9.5% of structural hemoglobinopathies. The majority of these unstable variants are the result of gene point mutations resulting in the substitution of a single amino acid by another. The presence of two mutations in the same allele is infrequent: of the 781 variants of the β-globin cluster described, only 32 are due to two point mutations (4.1%). Hb Extremadura is a structural variant that is included within the so-called unstable Hb anomalies. It was first described in 1989, employing the most up-to-date techniques available at that time, reversed phase high performance liquid chromatography (HPLC) to separate the abnormal chain (β(X)) digesting it with trypsin and analysis of the fragments with an automatic analyzer.

摘要

相似文献

1
Hb Extremadura [β64(E8)Gly→Ser;β133(H11)Val→Leu]: a new molecular analysis.
Hemoglobin. 2011;35(4):423-7. doi: 10.3109/03630269.2011.576353.
2
Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.与一种新的高度不稳定α珠蛋白变体(Hb 伊拉克利翁,α1cd37(C2)Pro>0)相关的独特表型表达:与其他α地中海贫血血红蛋白病的比较。
Blood Cells Mol Dis. 2000 Aug;26(4):276-84. doi: 10.1006/bcmd.2000.0307.
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Hb Marineo [beta70(E14)Ala-->Val]: a silent hemoglobin variant with a mutation within the heme pocket.Hb Marineo [β70(E14)丙氨酸→缬氨酸]:一种血红素袋内发生突变的沉默血红蛋白变体。
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Hemoglobin. 2016 Jun;40(3):143-9. doi: 10.3109/03630269.2016.1150292. Epub 2016 Mar 31.
6
Hb Phimai [β72(E16)Ser→Thr]: a novel β-globin structural variant found in association with Hb constant spring in pregnancy.披迈血红蛋白[β72(E16)丝氨酸→苏氨酸]:一种与孕期血红蛋白恒河猴相关的新型β珠蛋白结构变异体。
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Strategy for identification by mass spectrometry of a new human hemoglobin variant with two mutations in Cis in the beta-globin chain: Hb S-Clichy [beta6(A3)Glu-->Val; beta8(A5)Lys-->Thr].通过质谱鉴定β-珠蛋白链中存在两个顺式突变的新型人类血红蛋白变体的策略:Hb S-克利希[β6(A3)谷氨酸→缬氨酸;β8(A5)赖氨酸→苏氨酸]
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Co-inheritance of Hb Hershey [beta70(E14) Ala-->Gly] and Hb La Pommeraie [beta133(H11)Val-->Met] in a Sicilian subject.在一位西西里岛居民中共同遗传的 Hb Hershey [β70(E14)Ala→Gly]和 Hb La Pommeraie [β133(H11)Val→Met]。
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Further studies on Hb Canebière [β12(G4)Asn→His], a low affinity hemoglobin variant.对低亲和力血红蛋白变体Hb Canebière [β12(G4)天冬酰胺→组氨酸]的进一步研究。
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引用本文的文献

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Hb Cibeles [α2 CD25(B6) (Gly → Asp)]: a novel alpha chain variant causing alpha-thalassemia.希贝莱斯血红蛋白[α2 CD25(B6)(甘氨酸→天冬氨酸)]:一种导致α地中海贫血的新型α链变体。
Int J Hematol. 2014 Dec;100(6):599-601. doi: 10.1007/s12185-014-1663-2. Epub 2014 Sep 12.