An abnormal human hemoglobin was found in a hemolysate from a 5-year-old healthy child living in Prato (Tuscany, Italy). Structural studies demonstrated a previously unreported amino acid substitution, α31 (B12) Arg → Ser (this is an α 1β1 contact). The new variant has been named Hb Prato. It was unstable in isopropanol and heat-denaturation tests, but has normal functional properties, with respect to whole blood studies. Family studies indicated that the variant had been inherited from the mother, a 39-year-old woman of Sicilian extraction. Hb Prato occurs at 20 and 28% in hemolysates from the boy and woman, respectively. © 1979
Hemoglobinopathies, the disorders of hemoglobin structure and synthesis, can be divided into two for...
Hb Cardarelli [β86(F2)Ala → Pro] is a new unstable and high oxygen affinity variant found in several...
AbstractA new β-variant has been detected and structurally defined in a French male, with a life-lon...
An α-chain variant hemoglobin was found in the hemolysate of a 21-year-old healthy male living in Ba...
An abnormal human hemoglobin was found in association with β-thalassemia in a hemolysate from an 11-...
An abnormal, fast moving hemoglobin was noted in a 34-yr-old male patient living in Legnano (norther...
During a screening program for the identification of β-thalassemia (β-thal) carriers in Sardinia, It...
During a survey for abnormal hemoglobins in Polesine (a region north of the Po river, where betathal...
International audienceHb Dompierre [β29(B11)Gly→Arg, HBB: c.88G>C] is a rare β-globin gene variant t...
Hb J Calabria is a fast moving hemoglobin variant which was found in an Italian family by Vecchio et...
A new variant of hemoglobin M (Hb M) was discovered from a family of hereditary cyanosis living in A...
Two healthy newborns, heterozygous for two different Y-globin chain mutations, were observed during...
This study describes a new molecular condition in the α2- globin gene (HBA2) found in six unrelated ...
Hb Okazaki [β93(F8)Cys-Arg], was first described in 1984 as unstable hemoglobin variant having high ...
A high oxygen affinity hemoglobin (Hb) variant, Hb J-Cape Town [α92(FG4)Arg→Gln (α1), CGG→CAG] was i...
Hemoglobinopathies, the disorders of hemoglobin structure and synthesis, can be divided into two for...
Hb Cardarelli [β86(F2)Ala → Pro] is a new unstable and high oxygen affinity variant found in several...
AbstractA new β-variant has been detected and structurally defined in a French male, with a life-lon...
An α-chain variant hemoglobin was found in the hemolysate of a 21-year-old healthy male living in Ba...
An abnormal human hemoglobin was found in association with β-thalassemia in a hemolysate from an 11-...
An abnormal, fast moving hemoglobin was noted in a 34-yr-old male patient living in Legnano (norther...
During a screening program for the identification of β-thalassemia (β-thal) carriers in Sardinia, It...
During a survey for abnormal hemoglobins in Polesine (a region north of the Po river, where betathal...
International audienceHb Dompierre [β29(B11)Gly→Arg, HBB: c.88G>C] is a rare β-globin gene variant t...
Hb J Calabria is a fast moving hemoglobin variant which was found in an Italian family by Vecchio et...
A new variant of hemoglobin M (Hb M) was discovered from a family of hereditary cyanosis living in A...
Two healthy newborns, heterozygous for two different Y-globin chain mutations, were observed during...
This study describes a new molecular condition in the α2- globin gene (HBA2) found in six unrelated ...
Hb Okazaki [β93(F8)Cys-Arg], was first described in 1984 as unstable hemoglobin variant having high ...
A high oxygen affinity hemoglobin (Hb) variant, Hb J-Cape Town [α92(FG4)Arg→Gln (α1), CGG→CAG] was i...
Hemoglobinopathies, the disorders of hemoglobin structure and synthesis, can be divided into two for...
Hb Cardarelli [β86(F2)Ala → Pro] is a new unstable and high oxygen affinity variant found in several...
AbstractA new β-variant has been detected and structurally defined in a French male, with a life-lon...