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Hemoglobin
international journal for hemoglobin research
Volume 39, 2015 - Issue 2
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Original Article

A New Krüppel-Like Factor 1 Mutation (c.947G > A or p.C316Y) in Humans Causes β-Thalassemia Minor

Takenori NittaDepartment of Health Science, Yamaguchi University Graduate School of Medicine, Ube, Japan, Correspondence[email protected]
,
Fumio KawanoDepartment of Hematology, National Hospital Organization, Kumamoto Medical Center, Kumamoto, Japan,
,
Yasuhiro YamashiroDepartment of Health Science, Yamaguchi University Graduate School of Medicine, Ube, Japan,
,
Fumiya TakagiDepartment of Clinical Laboratory, Fukuyama Medical Center, Fukuyama, Japan,
,
Tomoaki MurataAnimal Experimental Department, Comprehensive Scientific Research Center, Yamaguchi University,
,
Tatehiko TanakaDepartment of Health Science, Yamaguchi University Graduate School of Medicine, Ube, Japan,
,
Mella FeraniaDepartment of Health Science, Yamaguchi University Graduate School of Medicine, Ube, Japan,
,
Chris AdhiyantoFaculty of Medicine and Health Science, Universitas Islam Negeri Syarif Hidayatullah, Jakarta, Indonesia, and
&
Yukio HattoriDepartment of Clinical Laboratory, Saiseikai Yamaguchi General Hospital, Yamaguchi, Japan
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Pages 121-126 | Received 27 Jul 2014, Accepted 09 Sep 2014, Published online: 18 Feb 2015

Citations (8)

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Read on this site (3)

Ahmad Tamaddoni, Sahar Khabaz Astaneh, Reza Tabaripour & Haleh Akhavan-Niaki. (2019) Krüppel-Like Factor 1 Gene Mutations in Thalassemia Patients from North Iran: Report of a New Mutation Associated with β-Thalassemia Intermedia. Hemoglobin 43:1, pages 12-17.
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Pegah Adelvand, Mohammed Hamid & Soroush Sardari. (2018) The intrinsic genetic and epigenetic regulator factors as therapeutic targets, and the effect on fetal globin gene expression. Expert Review of Hematology 11:1, pages 71-81.
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Ferania Mella, Yasuhiro Yamashiro, Chris Adhiyanto, Tatehiko Tanaka, Takenori Nitta, Yuki Amao & Masafumi Kimoto. (2018) A Coincidental Discovery of a New Stable Variant (Hb Hachioji or HBB: c.187C>T) in a Patient with Chronic Hemolytic Anemia of Unexplained Origin. Hemoglobin 42:1, pages 1-6.
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Articles from other publishers (5)

Ravindra Kumar, Rajiv Yadav, Sweta Mishra, M. P. S. S. Singh, Anil Gwal, Praveen K. Bharti & Shanmugam Rajasubramaniam. (2021) Krüppel-like factor 1 (KLF1) gene single nucleotide polymorphisms in sickle cell disease and its association with disease-related morbidities. Annals of Hematology 100:2, pages 365-373.
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Barbara J. Bain. 2020. Haemoglobinopathy Diagnosis. Haemoglobinopathy Diagnosis 1 29 .
L.‐Y. Huang, J. Li, Y. Zhang & D.‐Z. Li. (2018) A KLF 1 gene mutation causes β‐thalassemia minor in a Chinese family . International Journal of Laboratory Hematology 40:2.
Crossref
Andrew Perkins, Xiangmin Xu, Douglas R. Higgs, George P. Patrinos, Lionel ArnaudJames J. Bieker & Sjaak Philipsen. (2016) Krüppeling erythropoiesis: an unexpected broad spectrum of human red blood cell disorders due to KLF1 variants. Blood 127:15, pages 1856-1862.
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Maria Elisabetta Paglietti, Stefania Satta, Maria Carla Sollaino, Susanna Barella, Arianna Ventrella, Maria Franca Desogus, Franca Rosa Demartis, Laura Manunza & Raffaella Origa. (2016) The Problem of Borderline Hemoglobin A2 Levels in the Screening for β-Thalassemia Carriers in Sardinia. Acta Haematologica 135:4, pages 193-199.
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