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Hemoglobin
international journal for hemoglobin research
Volume 43, 2019 - Issue 4-5
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Original Articles

Genetic Background of β-Thalassemia in Northeast Algeria with Assessment of the Thalassemia Severity Score and Description of a new β0-Thalassemia Frameshift Mutation (HBB: c.374dup; p.Pro126Thrfs*15)

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Pages 223-228 | Received 05 Sep 2019, Accepted 17 Sep 2019, Published online: 11 Oct 2019

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Read on this site (2)

Saddam Hossain & M. Sadik Batcha. (2021) A Scientometric Analysis and Visualization on Beta Thalassemia Research at Global Perspectives. Journal of Hospital Librarianship 21:4, pages 391-404.
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Aisha Moeen Khan, Asma Mohammed Al-Sulaiti, Salma Younes, Mohamed Yassin & Hatem Zayed. (2021) The spectrum of beta-thalassemia mutations in the 22 Arab countries: a systematic review. Expert Review of Hematology 14:1, pages 109-122.
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Articles from other publishers (6)

Ekta Rao, Sandip Kumar Chandraker, Mable Misha Singh & Ravindra Kumar. (2024) Global distribution of β-thalassemia mutations: An update. Gene 896, pages 148022.
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Narmeen Ahmad, Hersh Karim, Luqman Rasool, Khanzad Ali, Mohammed Mahmood, Tara Osman & Chawan Hamakhan. (2023) A SPECTRUM OF Β-THALASSEMIA MUTATIONS IN SULAIMANI PROVINCE OF IRAQ: IDENTIFICATION OF NOVEL MUTATIONS. JOURNAL OF SULAIMANI MEDICAL COLLEGE 13:4, pages 7.
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Ihab Belmokhtar, Saida Lhousni, Mounia Elidrissi Errahhali, Ayad Ghanam, Manal Elidrissi Errahhali, Zaina Sidqi, Meryem Ouarzane, Majida Charif, Mohammed Bellaoui, Redouane Boulouiz & Noufissa Benajiba. (2022) Molecular heterogeneity of β‐thalassemia variants in the Eastern region of Morocco. Molecular Genetics & Genomic Medicine 10:8.
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Sergio Felipe Pinzón Mariño, Paloma Ropero Gradilla, Fernando Ataulfo González Fernández, Ana María Villegas Martínez, Silvia Méndez Martínez, Francisco de Asís Bartol Puyal, Elisa Viladés Palomar, Carlos Isanta Otal, Beatriz Cordón Ciordia, Josep Oriol Casanovas Marsal, Samira Bakali Badesa, José Alejando García Ortego, Ana Gómez Martínez, María Ángeles Montañés Gracia & Valle Recasens. (2021) Sickle cell disease associated with thalassemia; description of a rare mutation. Clinical Biochemistry 94, pages 80-82.
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Thongperm Munkongdee, Sissades Tongsima, Chumpol Ngamphiw, Pongsakorn Wangkumhang, Chayanon Peerapittayamongkol, Hafizah Binti Hashim, Suthat Fucharoen & Saovaros Svasti. (2021) Predictive SNPs for β0-thalassemia/HbE disease severity. Scientific Reports 11:1.
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Shuang-Ping Ma, Hai-Rui Xi, Xu-Xia Gao, Jing-Min Yang, Ryo Kurita, Yukio Nakamura, Xian-Min Song, Hong-Yan Chen & Da-Ru Lu. (2021) Long noncoding RNA HBBP1 enhances γ-globin expression through the ETS transcription factor ELK1. Biochemical and Biophysical Research Communications 552, pages 157-163.
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