A novel frameshift mutation at codon 66 (HBB:c.del201A) in the β-globin gene leads to beta-thalassemia

Nae Yu; Hye Ryoun Kim; Young Joo Cha; Eun Kyung Park

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A novel frameshift mutation at codon 66 (HBB:c.del201A) in the β-globin gene leads to beta-thalassemia

机译：β-珠蛋白基因中第66位密码子（HBB：c.del201A）的新型移码突变导致β地中海贫血

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《Annals of Hematology》 |2011年第2期|p.243-244|共2页
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Nae Yu; Hye Ryoun Kim; Young Joo Cha; Eun Kyung Park;
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1. A novel frameshift mutation at codon 66 (HBB:c.del201A) in the beta-globin gene leads to beta-thalassemia. [J] . Yu N, Kim HR, Cha YJ, Annals of hematology . 2011,第2期

机译：β-珠蛋白基因中第66位密码子（HBB：c.del201A）的新型移码突变导致β地中海贫血。
2. A Novel Frameshift Mutation at Codons 138/139 (HBB: c.417_418insT) on the -Globin Gene Leads to -Thalassemia [J] . Jiang Fan, Huang Lv-Yin, Chen Gui-Lan, Hemoglobin: International Journal for Hemoglobin Research . 2017,第1a6期

机译：在-Globin基因138/139（HBB：C.417_418Inst）上的小型帧突变导致-Thalassemia
3. A Novel Frameshift Mutation at Codon 2 (-T) {HBB: c.9delT) and First Report of Three New beta-Globin Mutations From Azerbaijan [J] . Bayram Bayramov, Gunay Aliyeva, Chingiz Asadov Hemoglobin: International Journal for Hemoglobin Research . 2019,第1a6期

机译：Codon 2（-T）{HBB：C.9delt）的新型帧突变突变，以及来自阿塞拜疆的三种新的β-珠蛋白突变的第一报告
4. Screening of β-Globin Gene Mutations in Adolescent Schoolgirls in Rural Malang and Sukabumi City, Java Province, Indonesia [C] . Chris Adhiyanto, Yanti Susianti, Nurlaely M. Rahmawati, International Integrative Conference on Health, Life and Social Sciences . 2018

机译：印度尼西亚爪哇省玛琅和苏克比乌市青少年女生β-珠蛋白基因突变的筛选
5. Targeted gene repair of frameshift mutations: Insights into the mechanism and applications for gene therapy [D] . Maguire, Katie K. 2007

机译：移码突变的靶向基因修复：深入了解基因治疗的机制和应用
6. A Novel Frameshift Mutation Deletion of HBB:c.199_202delAAAG Codon 66/67 (-AAAG) in β-Thalassemia Major Patients from the Western Region of Uttar Pradesh India [O] . Waseem Chauhan, Mohammad Afzal, Zeeba Zaka-ur-Rab, 2021

机译：一种新的框架突变缺失HBB：C.199_202DelaAG Codon 66/67（-AAAG）在印度北方邦西部的β-山西血症主要患者中
7. Nonsense codon mutations in the terminal exon of the beta-globin gene are not associated with a reduction in beta-mRNA accumulation: a mechanism for the phenotype of dominant beta-thalassemia [O] . GW Hall, S Thein 1994

机译：β-珠蛋白基因的末端外显子中的非阵容密码子突变与β-mRNA积累的还原无关：显性β-地中海贫血的表型的机制

A novel frameshift mutation at codon 66 (HBB:c.del201A) in the β-globin gene leads to beta-thalassemia

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