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Hemoglobin
international journal for hemoglobin research
Volume 25, 2001 - Issue 3
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Original

A NOVEL SPLICE ACCEPTOR SITE MUTATION OF THE α2-GLOBIN GENE CAUSING α-THALASSEMIA

Nélida I. Noguera Departamento Bioquímica Clínica. Area Hematología, Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, Rosario, 2000, Argentina
,
Fernando A. González Hospital Universitario San Carlos, Servicio de Hematología y Hemoterapia, Madrid, 28040, Spain
,
Rubén A. Dávoli Departamento Bioquímica Clínica. Area Hematología, Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, Rosario, 2000, Argentina
,
Angela C. Milani Departamento Bioquímica Clínica. Area Hematología, Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, Rosario, 2000, Argentina
&
Professor Ana Villegas Hospital Universitario San Carlos, Jefe de Servicio de Hematologia y Hemoterapia, c/Professor Martin Lagos s/n, Madrid, 28040, Spain; Hospital Universitario San Carlos, Servicio de Hematología y Hemoterapia, Madrid, 28040, Spain
Pages 311-315 | Received 07 Dec 2000, Published online: 07 Jul 2009

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Samaneh Farashi, Shadi Vakili, Negin F. Garous, Mehri Ashki, Hashem Imanian, Azita Azarkeivan & Hossein Najmabadi. (2015) Mutations on the α2-Globin Gene That May Trigger α+-Thalassemia. Hemoglobin 39:6, pages 398-402.
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Ita M. Nainggolan, Alida Harahap, Debby D. Ambarwati, Rosalina V. Liliani, Dewi Megawati, Maria Swastika & Iswari Setianingsih. (2013) Interaction of Hb Adana (HBA2: c.179G>A) with Deletional and Nondeletional α+-Thalassemia Mutations: Diverse Hematological and Clinical Features. Hemoglobin 37:3, pages 297-305.
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Karen G. Scheps, Amanda Binaghi & Viviana Varela. (2012) Identification of a New HBA1 Gene Mutation (HBA1:c.301-2A>T) in Cis with Hb Riccarton (HBA1:c.154G>A) [α51(CE9)Gly→Ser]. Hemoglobin 36:5, pages 504-507.
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Majid Yavarian, Mehran Karimi, Amine Zorai, Cornelis L Harteveld & Piero C Giordano. (2005) Molecular Basis of Hb H Disease in Southwest Iran. Hemoglobin 29:1, pages 43-50.
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Articles from other publishers (7)

Norafiza Mohd Yasin, Faidatul Syazlin Abdul Hamid, Syahzuwan Hassan, Yuslina Mat Yusoff, Ermi Neiza Mohd Sahid & Ezalia Esa. (2023) Characterization of New Alpha Zero (α0) Thalassaemia Deletion (−−GB) among Malays in Malaysian Population. Diagnostics 13:20, pages 3286.
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Mara Jorgelina Ojeda, Susana Mabel Perez, Arianna Flavia Pratti, Karina Lucrecia Calvo, Mariana Paula Raviola, María Eda Voss, Gladis Marcela Williams, Nélida Inés Noguera, María Magdalena Carbonell, Mónica Teresita Aixalá & Irma Margarita Bragós. (2016) Alpha Hemoglobinophaties in Rosario, Argentina. Thalassemia Reports 7:1, pages 5655.
Crossref
Samaneh Farashi & Hossein Najmabadi. (2015) Diagnostic pitfalls of less well recognized HbH disease. Blood Cells, Molecules, and Diseases 55:4, pages 387-395.
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Cornelis L Harteveld & Douglas R Higgs. (2010) α-thalassaemia. Orphanet Journal of Rare Diseases 5:1.
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Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. Weatherall. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 241 265 .
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallDouglas R. Higgs. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 239 240 .
C.L. Harteveld, M. Yavarian, A. Zorai, E.D. Quakkelaar, P. van Delft & P.C. Giordano. (2003) Molecular spectrum of α‐thalassemia in the Iranian population of Hormozgan: Three novel point mutation defects. American Journal of Hematology 74:2, pages 99-103.
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