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Hemoglobin
international journal for hemoglobin research
Volume 42, 2018 - Issue 3
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Original Article

A Novel β-Thalassemia Mutation in a Chinese family: IVS-II-203-205 (TCT>CC) (HBB: c.315+203TCT>CC)

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Pages 159-160 | Received 24 May 2018, Accepted 25 Jun 2018, Published online: 25 Sep 2018

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (2)

Wen-Juan Wang, Zi-Xuan Ding, Hui-Min Zhang, Ting-Ting Tao, Su-Ning Chen & Ling Xi. (2021) Identification of a Novel β-Thalassemia Mutation at Codon 130 (+T) (HBB: c.391insT) in Han Chinese . Hemoglobin 45:1, pages 46-48.
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Junkun Chen, Shaobin Lin, Jinghui Gan, Xiaoqin Xin & Jungao Huang. (2020) A novel β-thalassemia variant at HBB:c.14delC (Codon 4, -C) identified via next-generation sequencing. Hematology 25:1, pages 400-404.
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Articles from other publishers (3)

Hossein Jalali, Mahan Mahdavi, Mohammad Eslamijouybari & Mohammad Reza Mahdavi. (2023) Coinheritance of the c.-19 G > C and c.315 + 1 G > A Variants in the β-Globin Gene Leads to Thalassemia Disease: A Report from the North of Iran. Case Reports in Genetics 2023, pages 1-4.
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Jungao Huang, Le Ding, Junkun Chen, Shiping Chen, Peirun Tian, Jun Xie, Xiaoyan Huang & Xiaoqin Xin. (2022) Characterization of a novel HBB:c.194dup variant of the β -globin gene combined with six alpha genes . Journal of International Medical Research 50:5, pages 030006052210990.
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Jianlong Zhuang, Yu Zheng, Yuanbai Wang, Qianmei Zhuang, Yuying Jiang, Qingyue Xie, Shuhong Zeng & Jianxing Zeng. (2020) Identification of a new β-thalassaemia variant Term CD+32(HBB: c.32A>C) in two Chinese families. Journal of Clinical Pathology 73:9, pages 593-596.
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