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Hemoglobin
international journal for hemoglobin research
Volume 36, 2012 - Issue 4
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Short Communication

The +1,506 (A>C) Mutation in the 3′ Untranslated Region Affects β-Globin Expression

Minako Hino Faculty of Health Sciences, Yamaguchi University Graduate School of Medicine, Ube, Japan; United Arab Emirates Genetic Disease Association, Dubai, United Arab EmiratesCorrespondence[email protected]
,
Hitomi Ito Faculty of Health Sciences, Yamaguchi University Graduate School of Medicine, Ube, Japan
,
Yasuhiro Yamashiro Faculty of Health Sciences, Yamaguchi University Graduate School of Medicine, Ube, Japan
,
Yukio Hattori Faculty of Health Sciences, Yamaguchi University Graduate School of Medicine, Ube, Japan
,
Takenori Nitta Faculty of Health Sciences, Yamaguchi University Graduate School of Medicine, Ube, Japan
&
Chris Adhiyanto Faculty of Health Sciences, Yamaguchi University Graduate School of Medicine, Ube, Japan
Pages 399-406 | Received 28 Dec 2011, Accepted 12 Apr 2012, Published online: 26 Jun 2012

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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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Sogol Targholi, Zahra Noormohammadi, Elham Tafsiri & Morteza Karimipoor. (2022) Evaluation of the Function of a Rare Variant in the 3'-Untranslated Region of the β-Globin Gene. Hemoglobin 46:6, pages 312-316.
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Aditi Sen, Venu Seenappa, Prantar Chakrabarti & Tuphan Kanti Dolai. (2021) First Report of the 3'-Untranslated Region +1506 (A>C) [NM_000518.5: c.*32A>C] mutation on the β-Globin Gene in the Indian Population. Hemoglobin 45:5, pages 325-328.
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Takenori Nitta, Fumio Kawano, Yasuhiro Yamashiro, Fumiya Takagi, Tomoaki Murata, Tatehiko Tanaka, Mella Ferania, Chris Adhiyanto & Yukio Hattori. (2015) A New Krüppel-Like Factor 1 Mutation (c.947G > A or p.C316Y) in Humans Causes β-Thalassemia Minor. Hemoglobin 39:2, pages 121-126.
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Maria Ascensión Herrera, Félix De La Fuente-Gonzalo, Fernando Ataúlfo González, Jorge M. Nieto, Alejandra Blum Dominguez, Ana Villegas & Paloma Ropero. (2015) Identification of a Novel Mutation in the β-Globin Gene 3′ Untranslated Region (HBB: c.*+118A > G) in Spain. Hemoglobin 39:1, pages 30-35.
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Articles from other publishers (3)

Kok-Siong Poon, Evelyn Siew-Chuan Koay & Karen Mei-Ling Tan. (2021) Significance of variant annotation for molecular diagnosis of thalassaemia. Journal of Clinical Pathology 74:10, pages 676-677.
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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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