Rapid molecular characterization of mutations leading to unstable hemoglobin β-chain variants
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/BF01703113.pdf
Reference35 articles.
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4. Baudin-Chich V, Wajcman H, Gombaud-Saintonge G, Arous N, Riou J, Brière J, Galactéros F (1988) Hemoglobin Brest [β 127 (H5) Gln→Lys], a new unstable human hemoglobin variant located at the α 1 β 1 interface with specific electrophoretic behavior. Hemoglobin 12: 179–188
5. Beris P, Miescher PA, Diaz-Chico JC, Han IS, Kutlar A, Hu H, Wilson JB, Huisman THJ (1988) Inclusion body β-thalassemia trait in a Swiss family is caused by an abnormal hemoglobin (Geneva) with an altered and extended β-chain carboxy-terminus due to a modification in codon β 114. Blood 72: 801–805
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