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Hemoglobin
international journal for hemoglobin research
Volume 19, 1995 - Issue 3-4
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Original Article

A Novel Frameshift Mutation Causing β-Thalassemia in a Sikh

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Pages 183-189 | Received 18 Jul 1994, Accepted 07 Mar 1995, Published online: 07 Jul 2009

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Read on this site (5)

F. E. E. Vaz, C. B. Thakur(Mahadik)M. K. Banerjee & S. G. Gangal. (2000) Distribution of β-Thalassemia Mutations in the Indian Population Referred to a Diagnostic Center. Hemoglobin 24:3, pages 181-194.
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T. H. J. Huisman & M. F. H. Carver. (1998) The β-and -Thalassemia Repository (Ninth Edition; Part I). Hemoglobin 22:2, pages 169-195.
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S. El-Kalla & A. R. Mathews. (1997) A Novel β-Thalassemia Mutation [Codon 45 (-T)] in a Pakistani Family. Hemoglobin 21:6, pages 499-503.
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S. El-Kalla & A. R. Mathews. (1997) A Significant β-Thalassemia Heterogeneity in the United Arab Emirates. Hemoglobin 21:3, pages 237-247.
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E. Baysal & M. F. H. Carver. (1995) The β- and δ-Thalassemia Repository (Eighth Edition). Hemoglobin 19:3-4, pages 213-236.
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Articles from other publishers (7)

J. Da Luz, P. López, E. M. Kimura, D. M. Albuquerque, F. F. Costa, M. Sans & M. F. Sonati. (2012) A new β 0 ‐thalassemia frameshift mutation [β 48 (‐T)] in a Uruguayan family . International Journal of Laboratory Hematology 35:1, pages 111-114.
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S. Sinha, M. L. Black, S. Agarwal, R. Colah, R. Das, K. Ryan, M. Bellgard & A. H. Bittles. (2010) Profiling β-thalassaemia mutations in India at state and regional levels: implications for genetic education, screening and counselling programmes. The HUGO Journal 3:1-4, pages 51-62.
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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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D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
Roshan Colah & Dipika Mohanty. (1998) β-Thalassemias : Expression, molecular mechanisms and mutations in Indians. The Indian Journal of Pediatrics 65:6, pages 815-823.
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A.R. Pawar, R.B. Colah & D. Mohanty. (1997) A Novel β+-Thalassemia Mutation (Codon 10 GCC → GCA) and a Rare Transcriptional Mutation (−28A → G) in Indians. Blood 89:10, pages 3888-3888.
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A.R. Pawar, R.B. Colah & D. Mohanty. (1997) A Novel β+-Thalassemia Mutation (Codon 10 GCC → GCA) and a Rare Transcriptional Mutation (−28A → G) in Indians. Blood 89:10, pages 3888-3888.
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