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0029871464
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Hemoglobin Debrousse [β96(FG3)Leug→Pro]: A new unstable hemoglobin with twofold increased oxygen affinity
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0028838819
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A new α chain variant Hb Sallanches [α2 104(G11)Cys→Tyr] associated with Hb H disease in one homozygous patient
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Exonic splicing enhancers: Mechanism of action, diversity and role in human genetic diseases
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8
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0017028293
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Hb Henri Mondor: β26(B8)Glu→Val: A variant with a substitution localized at the same position as that of Hb E β26 Glu→Lys
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226(B8)Glu→Val
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0029750172
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Hb Aubenas [β26(B8)Glu→Gly]: A new variant normally synthetized, affecting the same codon as in Hb E
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11
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0020376275
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Abnormal RNA processing due to the exon mutation of the βE-globin gene
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Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia
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13
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0017603934
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Hemoglobin Lufkin: β29(B11)Gly→Asp. An unstable hemoglobin variant involving an internal amino acid residue
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0029125359
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Hb S-Hb Lufkin disease in a black male infant
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Hemoglobin Lufkin [β29(B11)Gly→Asp] in a Japanese
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