Unstable alpha-chain hemoglobin variants with factitious beta-thalassemia biosynthetic ratio: Hb questembert (α131[H14] Ser→Pro) and Hb Caen (α132[H15] Val→Gly)-Reference-Cited by-同舟云学术

Unstable alpha-chain hemoglobin variants with factitious beta-thalassemia biosynthetic ratio: Hb questembert (α131[H14] Ser→Pro) and Hb Caen (α132[H15] Val→Gly)

Published:1993-04 Issue:4 Volume:42 Page:367-374
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Wajcman H.,Vasseur C.,Blouquit Y.,Rosa J.,Labie D.,Najman A.,Reman O.,Leporrier M.,Galacteros F.

Publisher

Wiley

Subject

Hematology

Reference21 articles.

1. Unstable Hemoglobins

2. : Electrophoretic mobilities of mutant hemoglobins and mutant globin chains. In (eds): “CRC Handbook Series in Clinical Laboratory Science, Section I: Hematology, Vol. IV.” Boca Raton, FL: CRC Press, 1986.

3. Characterization Approach of ‘Silent’ Beta-Chain Hemoglobin Variants

4. ANALYTICAL AND PREPARATIVE ISOELECTRIC FOCUSING IN GEL-STABILIZED LAYERS

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2. Red blood cells free α-haemoglobin pool: a biomarker to monitor the β-thalassemia intermedia variability. The ALPHAPOOL study;British Journal of Haematology;2017-06-23

3. Hemoglobin variants – pathomechanism, symptoms and diagnosis;LaboratoriumsMedizin;2016-01-12

4. Description of Three NewαVariants and Four NewβVariants: Hb Montluel [α110(G17)Ala → Val;HBA1: c.332C > T], Hb Cap d’Agde [α131(H14)Ser → Cys;HBA2: c.395C > G] and Hb Corsica [α100(G7)Leu → Pro;HBA1: 302T > C]; Hb Nîmes [β104(G6)Arg → Gly;HBB: c.313A > G], Hb Saint Marcellin [β112(G14)Cys → Gly;HBB: c.337T > G], Hb Saint Chamond [β80(EF4)Asn → 0;HBB: c.241_243delAAC] and Hb Dompierre [β29(B11)Gly → Arg;HBB: c.88G > C];Hemoglobin;2015-05-04

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