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Article

Hb Evora [alpha 2-35, Ser-->Pro], a novel hemoglobin variant associated with an alpha-thalassemia phenotype.

Haematologica - 1 May 2007

Waye J S, Chui D H K

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Share to alpha-Thalassemia
Share to Genetic Variation
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 17562600
DOI: 10.3324/haematol.11572

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Related research

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Hb Evora [alpha 2-35, Ser-->Pro], a novel hemoglobin variant associated with an alpha-thalassemia phenotype.PMID 17562600Read ↗

Hb Evora [alpha2-35 (B16), Ser-->Pro], a novel hemoglobin variant associated with an alpha-thalassemia phenotype.Semantic proximity Read ↗

Description of Hb Évora (HBA2: c.106T>C) on an Unexpected Allele in a Swiss Family.Semantic proximity Read ↗

Hb Antalya [codons 3-5 (Leu-Thr-Pro-->Ser-Asp-Ser)]: a new unstable variant leading to chronic microcytic anemia and high Hb A2.Semantic proximity Read ↗

Hb Sögn or alpha 2 beta 2 14(A11)Leu-->Arg in combination with an alpha-thalassemia heterozygosity.Semantic proximity Read ↗

A novel beta-globin mutation (HBB:c.107A>G; or codon 35 beta (A-->G)) at alpha-beta chain interfaces.Semantic proximity Read ↗

Hb I-Toulouse [beta 66(E10)Lys->Glu] in association with alpha-thalassemia.Semantic proximity Read ↗

Four new variants of the alpha2-globin gene without clinical or hematologic effects: Hb Park Ridge [alpha9(alpha7)Asn-->Lys (alpha2)], Hb Norton [alpha72(EF1)His-->Asp (alpha2)], Hb Lombard [alpha103(G10)His-->Tyr (alpha2)], and Hb San Antonio [A113(GH2)Leu-->Arg (A2)].Semantic proximity Read ↗

A novel Indian beta-thalassemia mutation: Hb Lucknow [beta8(A5)Lys-->Arg]].Semantic proximity Read ↗

Hb Roubaix [alpha55(E4)Val-->Leu]: a new neutral hemoglobin variant involving the alpha1 gene.Semantic proximity Read ↗

Sickle-cell anemia hemoglobin: the molecular biology of the first "molecular disease"--the crucial importance of serendipity.Semantic proximity Read ↗

A novel beta-globin variant: Hb Poços de Caldas [beta 61(E5)Lys-->Gln].Semantic proximity Read ↗

Severe Hb S-beta+ thalassemia caused by IVS-I splice site mutations.Semantic proximity Read ↗

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