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Hemoglobin ; 26(1): 1-5, 2002 Feb.
Article in English | MEDLINE | ID: mdl-11939506

ABSTRACT

We report a novel mutation, Hb A2-Monreale [delta146(HC3)His-->Arg], detected by cation exchange high performance liquid chromatography in a family from West Sicily. The mutation is due to a CAT-->CGT substitution at codon 146 of the delta-globin gene. The two carriers had reduced levels of normal Hb A2 (1.1%), but comparable levels (0.9%) of the Hb A2 variant. Most likely the new variant has the same characteristics as Hb Cochin-Port Royal [beta146(HC3)His-->Arg], that is stable but has a 75% reduction of the Bohr effect. The finding of the new variant increases the genotype heterogeneity of the delta-globin gene in the Mediterranean area, and is relevant to the study and prevention of Cooley's Anemia.


Subject(s)
Amino Acid Substitution , Codon/genetics , Globins/genetics , Hemoglobins, Abnormal/isolation & purification , Mutation, Missense , Point Mutation , Adult , Alleles , Chromatography, High Pressure Liquid , DNA Mutational Analysis , False Positive Reactions , Female , Genotype , Hemoglobins, Abnormal/chemistry , Hemoglobins, Abnormal/genetics , Humans , Male , Mass Screening , Middle Aged , Polymorphism, Restriction Fragment Length , Sicily/epidemiology , beta-Thalassemia/diagnosis , beta-Thalassemia/epidemiology
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