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Hemoglobin
international journal for hemoglobin research
Volume 36, 2012 - Issue 6
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Original Article

Hb Iberia [α104(G11)Cys → Arg,TGC>CGC (α2) (HBA2:c.313T>C)], a New α-Thalassemic Hemoglobin Variant Found in the Iberian Peninsula: Report of Six Cases

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Pages 517-525 | Received 17 Apr 2012, Accepted 24 Jul 2012, Published online: 27 Nov 2012

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Elizabete Cunha, Celeste Bento, Ana Oliveira, Luís Relvas, Joana Neves, Mariline Gameiro, Cristina Barros, Ana Araújo, Ana Macedo, Paula Rocha, Ricardo Costa, Tabita Maia & M. Letícia Ribeiro. (2013) Hb Plasencia [α125(H8)Leu→Arg (α2)] is a Frequent Cause of α+-Thalassemia in the Portuguese Population. Hemoglobin 37:2, pages 183-187.
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Chris E. Cooper, Matthew Bird, XiaoBo Sheng, Ji-Won Choi, Gary G.A. Silkstone, Michelle Simons, Natalie Syrett, Riccardo Piano, Luca Ronda, Stefano Bettati, Gianluca Paredi, Andrea Mozzarelli & Brandon J. Reeder. (2021) Stability of Maleimide-PEG and Mono-Sulfone-PEG Conjugation to a Novel Engineered Cysteine in the Human Hemoglobin Alpha Subunit. Frontiers in Chemistry 9.
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