Citations (6)
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Yun-Jing Wen, Qiu-Xia Yu, Fan Jiang & Dong-Zhi Li. (2022) Identification of a Novel Mutation in the 3′ Untranslated Region of the β-Globin Gene (HBB:c.*132C>G) in a Chinese Family. Hemoglobin 46:6, pages 347-350.
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Fan Jiang, Gui-Lan Chen, Jian Li, Xue-Wei Tang & Dong-Zhi Li. (2022) β-Thalassemia Intermedia Caused by the β-Globin Gene 3′ Untranslated Region: Another Case Report. Hemoglobin 46:2, pages 137-139.
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Articles from other publishers (4)
Phan Thị Xinh, Ho Quoc Chuong, Nguyen Thi Thanh Ha, Huynh Duong Bich Tram, Cao Van Dong, Le Vu Ha Thanh, Nguyen Thi Hong Hoa, Huynh Nghia, Nguyen Tan Binh, Phu Chi Dung & Hoang Anh Vu. (2022) Spectrum of HBB gene mutations among 696 β–thalassemia patients and carriers in Southern Vietnam. Molecular Biology Reports 49:4, pages 2601-2606.
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Stacy Colaco & Anita Nadkarni. (2021) Borderline HbA2 levels: Dilemma in diagnosis of beta-thalassemia carriers. Mutation Research/Reviews in Mutation Research 788, pages 108387.
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Adivitch Sripusanapan, Arunee Phusua, Kanda Fanhchaksai & Pimlak Charoenkwan. (2020)
Compound heterozygosity of a silent beta‐thalassemia mutation at the 3′‐untranslated region (
HBB
: c.*132 C>T) and beta‐zero thalassemia results in thalassemia intermedia
. Pediatric Blood & Cancer 67:4.
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M. Vinciguerra, C. Passarello, F. Cassarà, F. Leto, M. Cannata, G. Calvaruso, R. Di Maggio, D. Renda, A. Maggio & A. Giambona. (2016)
Co-heredity of silent CAP + 1570 T>C (
HBB
:c*96T>C) defect and severe β-thal mutation: a cause of mild β-thalassemia intermedia
. International Journal of Laboratory Hematology 38:1, pages 17-26.
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