Hb Ramona or alpha (2)24(B5)Tyr-->Cys beta 2.
作者信息
Pobedimskaya D D, Molchanova T P, Huisman T H
机构信息
Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta 30912-2100.
出版信息
Hemoglobin. 1994 Sep;18(4-5):365-6. doi: 10.3109/03630269408996205.
PMID:7852094
Abstract
摘要
相似文献
1
Hb Ramona or alpha (2)24(B5)Tyr-->Cys beta 2.血红蛋白拉蒙娜或α(2)24(β5)酪氨酸→半胱氨酸β2
Hemoglobin. 1994 Sep;18(4-5):365-6. doi: 10.3109/03630269408996205.
2
Hb Luxembourg [alpha 24(B5)Tyr----His], Hb Maputo [beta 47(CD6)Asp----Tyr], and Hb Fukuyama [beta 77(EF1)His----Tyr].
Hemoglobin. 1991;15(1-2):97-101. doi: 10.3109/03630269109072488.
3
Hb A2-Sant' Antioco [alpha 2 delta (2)93(F9)Cys-->Gly]: a new delta chain variant identified by sequencing of amplified DNA.血红蛋白A2-圣安蒂奥科[α2δ(2)93(F9)半胱氨酸→甘氨酸]：一种通过扩增DNA测序鉴定的新型δ链变体。
Hemoglobin. 1994 Nov;18(6):437-9. doi: 10.3109/03630269409045776.
4
Hb Canterbury [beta112(G14)Cys-->Phe]: a new, mildly unstable variant.血红蛋白坎特伯雷[β112（G14）半胱氨酸→苯丙氨酸]：一种新的轻度不稳定变体。
Hemoglobin. 2002 Feb;26(1):67-9. doi: 10.1081/hem-120002942.
5
Hb F-Veleta or alpha 2 G gamma(2)40(C6)Arg-->Gly.血红蛋白F-Veleta或α2Gγ(2)40（C6）精氨酸→甘氨酸
Hemoglobin. 1995;19(6):407-11.
6
Four new beta chain hemoglobin variants without clinical or hematological effects: Hb San Bruno [beta39(C5)Gln-->His]; Hb Fort Dodge [beta93(F9)Cys-Tyr]; Hb Rhode Island [beta116(G18)His-->Tyr]; and Hb Inglewood [beta142(H20)Ala-->Thr].四种无临床及血液学影响的新型β链血红蛋白变异体：圣布鲁诺血红蛋白[β39(C5)谷氨酰胺→组氨酸]；福特道奇血红蛋白[β93(F9)半胱氨酸-酪氨酸]；罗德岛血红蛋白[β116(G18)组氨酸→酪氨酸]；以及英格尔伍德血红蛋白[β142(H20)丙氨酸→苏氨酸]。
Hemoglobin. 2002 Aug;26(3):299-303. doi: 10.1081/hem-120015034.
7
Hb Ube-2 in a Taiwanese subject: an A-->G substitution at codon 68 of the alpha2-globin gene.一名台湾受试者中的血红蛋白Ube-2：α2-珠蛋白基因第68密码子处的A→G替换。
Hemoglobin. 2002 Feb;26(1):99-101. doi: 10.1081/hem-120002949.
8
Hb Sallanches [alpha104(G11)Cys-->Tyr, TGC-->TAC (alpha2)]: an unstable hemoglobin variant found in an Indian child.
Hemoglobin. 2006;30(3):393-6. doi: 10.1080/03630260600755872.
9
Hb Barika [alpha42(C7)Tyr-->His (alpha2)] leads to an alpha+ -Thalassemia-like syndrome.血红蛋白巴里卡[α42（C7）酪氨酸→组氨酸（α2）]导致一种α+地中海贫血样综合征。
Hemoglobin. 2007;31(1):17-22. doi: 10.1080/03630260601056833.
10
A new beta chain variant, Hb Vienna or beta77(EF1)His-->Gln.一种新的β链变体，血红蛋白维也纳或β77(EF1)组氨酸突变为谷氨酰胺。
Hemoglobin. 1998 Jul;22(4):391-5. doi: 10.3109/03630269809071535.
Zotero 插件