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Hemoglobin
international journal for hemoglobin research
Volume 26, 2002 - Issue 1
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A NOVEL β0-THALASSEMIA MUTATION AT CODON 55 (−A) AND A RARE 17 bp DELETION AT CODONS 126–131 IN THE INDIAN POPULATION

Anita Nadkarni Gene Dynamics Group, Institute of Molecular and Cell Biology, Institute of Advanced Industrial Science and Technology, Central 6, Higashi 1-1, Tsukuba, Ibaraki, 305-8566, Japan; Department of Hematogenetics, Institute of Immunohematology, ICMR, Mumbai, 400012, India
,
Takehisa Sakaguchi Gene Dynamics Group, Institute of Molecular and Cell Biology, Institute of Advanced Industrial Science and Technology, Central 6, Higashi 1-1, Tsukuba, Ibaraki, 305-8566, Japan; Department of Industrial Chemistry, Chiba Institute of Technology, Chiba, 275-0016, Japan
,
Hiroshi Takaku Department of Industrial Chemistry, Chiba Institute of Technology, Chiba, 275-0016, Japan
,
Ajit Gorakshakar Department of Hematogenetics, Institute of Immunohematology, ICMR, Mumbai, 400012, India
,
Supriya Phanasgaonkar Department of Hematogenetics, Institute of Immunohematology, ICMR, Mumbai, 400012, India
,
Roshan B. Colah Department of Hematogenetics, Institute of Immunohematology, ICMR, Mumbai, 400012, India
,
Dipika Mohanty Department of Hematogenetics, Institute of Immunohematology, ICMR, Mumbai, 400012, India
&
Ryoiti Kiyama Gene Dynamics Group, Institute of Molecular and Cell Biology, Institute of Advanced Industrial Science and Technology, Central 6, Higashi 1-1, Tsukuba, Ibaraki, 305-8566, Japan
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Pages 41-47 | Received 26 Jun 2001, Accepted 24 Aug 2001, Published online: 07 Jul 2009

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Snehadhini Dehury, Satyabrata Meher, Siris Patel, Kishalaya Das, Arpita Jana, Subhra Bhattacharya, Sarmila Sahoo, Biswanath Sarkar & Pradeep K. Mohanty. (2019) Compound Heterozygote of Hb S (HBB: c.20A>T)/Hb Westdale (HBB: c.380_396delTGCAGGCTGCCTATCAG): Report of Four Cases from Odisha State, India. Hemoglobin 43:2, pages 132-136.
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Eunice S. Edison, Rajkumar S. Venkatesan, Sankari Devi Govindanattar, Biju George & Ramachandran V. Shaji. (2012) A Novel 26 bp Deletion [HBB: c.20_45del26bp] in Exon 1 of the β-Globin Gene Causing β-Thalassemia Major. Hemoglobin 36:1, pages 98-102.
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Ajit C. Gorakshakar, Supriya P. Phanasgaonkar, Anita H. Nadkarni, Roshan B. Colah & Dipika Mohanty. (2004) Detection of Rare β‐Thalassemia Mutations by Denaturing Gradient Gel Electrophoresis Among Indians. Hemoglobin 28:1, pages 15-24.
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Articles from other publishers (12)

Poonam Tripathi, Sarita Agarwal, Anshul Gupta & Kausik Mandal. (2020) Biallelic rare 17 bp deletion mutation (HBB:c.380_396 del TGCAGGCTGCCTATCAG) in a transfusion depended form of thalassemia. Annals of Hematology 99:11, pages 2719-2722.
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Dong-Zhi Li, Can Liao, Jian Li & Ru Li. (2009) A novel β-globin gene deletion (codons 89–93) in a Chinese family. Annals of Hematology 89:3, pages 323-325.
Crossref
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallSwee Lay Thein & William G. Wood. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 323 356 .
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. Weatherall. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 321 322 .
Roshan Colah, Ajit Gorakshakar, Anita Nadkarni, Supriya Phanasgaonkar, Reema Surve, Pratibha Sawant, Dipika Mohanty & Kanjaksha Ghosh. (2009) Regional heterogeneity of β-thalassemia mutations in the multi ethnic Indian population. Blood Cells, Molecules, and Diseases 42:3, pages 241-246.
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A. Nadkarni, T. Sakaguchi, A. Gorakshakar, S. Phanasgaonkar, R. Colah, D. Mohanty & R. Kiyama. (2005) Three novel polymorphisms in the β globin gene. American Journal of Hematology 80:2, pages 161-163.
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Paloma Ropero, Ana Villegas, Miguel Martínez, Fernando Ataulfo González Fernández, Celina Benavente & Marta Mateo. (2005) A deletion of 11 bp (CD 131–134) in exon 3 of the β-globin gene produces the phenotype of inclusion body β-thalassemia. Annals of Hematology 84:9, pages 584-587.
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A. NADKARNI, T. SAKAGUCHI, A. GORAKSHAKAR, S. PHANASGAONKAR, R. KIYAMA, R. COLAH & D. MOHANTY. (2004) An interplay of alleviating mutations in the clinical phenotype of beta-thalassaemia intermedia. Clinical and Laboratory Haematology 26:6, pages 419-422.
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Roshan Colah, Anita Nadkarni, Ajit Gorakshakar, Supriya Phanasgaonkar, Reema Surve, P.G. Subramaniam, Nagnath Bondge, Kamala Pujari, Kanjaksha Ghosh & Dipika Mohanty. (2004) Impact of β globin gene mutations on the clinical phenotype of β thalassemia in India. Blood Cells, Molecules, and Diseases 33:2, pages 153-157.
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Anju Gupta & Sarita Agarwal. (2004) Rare β‐thalassemia mutations are cause of concern. American Journal of Hematology 76:3, pages 312-312.
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John Old. 2004. Genetic Disorders of the Indian Subcontinent. Genetic Disorders of the Indian Subcontinent 245 264 .
Christopher A. Fisher, Anuja Premawardhena, Shanthimala De Silva, Giathra Perera, Shabna Rajapaksa, Nancy A. Olivieri, John M. Old & David J. Weatherall. (2003) The molecular basis for the thalassaemias in Sri Lanka. British Journal of Haematology 121:4, pages 662-671.
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