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Hemoglobin
international journal for hemoglobin research
Volume 19, 1995 - Issue 1-2
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Original Article

Hb ananosa or α2111(G18)Ala → Valβ (α2 Mutation) and Hb mulhacen or α2123(H6)Ala → Serβ2 (αl Mutation) are two silent stable variants detected by sequencing of amplified dna

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Pages 1-6 | Received 16 Jun 1994, Accepted 11 Dec 1994, Published online: 07 Jul 2009

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Agathe Horri-Naceur & David J. Timson. (2020) In Silico Analysis of the Effects of Point Mutations on α-Globin: Implications for α-Thalassemia. Hemoglobin 44:2, pages 89-103.
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M. F. H. Carver & T. H. J. Huisman. (1997) International Hemoglobin Information Center Variant List. Hemoglobin 21:6, pages 505-506.
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. (1996) Variants of the Alpha Chain. Hemoglobin 20:3, pages 215-312.
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H. Wajcman, Y. Blouquit, A. Lahary, A. M. Soummer, P. Groff, J. Bardakdjian, C. Prehu, J. Riou, C. Godard & F. Galacteros. (1995) Three New Neutral A Chain Variants: Hb Bois Guillaume [α65(E14)Ala→Val], Hb Mantes-La-Jolie [α79(Ef8)Ala→T, and Hb Mosella [α111(G18)Ala→Thr]. Hemoglobin 19:5, pages 281-286.
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Articles from other publishers (1)

Karen G. Scheps, Marcia A. Hasenahuer, Gustavo Parisi, Héctor M. Targovnik & María S. Fornasari. (2019) Curating the gnomAD database: Report of novel variants in the globin‐coding genes and bioinformatics analysis. Human Mutation 41:1, pages 81-102.
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