A New δ Chain Variant, Hb A₂-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], Observed in a Tunisian Family in Association with a Compound Heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β⁰-Thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A]

Imen MoumniLaboratoire d’Hématologie Moléculaire et Cellulaire, Institut Pasteur TunisTunisieCorrespondence[email protected]

Amine ZoraiLaboratoire d’Hématologie Moléculaire et Cellulaire, Institut Pasteur TunisTunisie

Sonia MahjoubLaboratoire d’Hématologie, CHU La Rabta La RabtaTunisie

Ikbel MosbahiLaboratoire d’Hématologie Moléculaire et Cellulaire, Institut Pasteur TunisTunisie

Dorra ChaouechiLaboratoire d’Hématologie Moléculaire et Cellulaire, Institut Pasteur TunisTunisie

Neila BenromdhaneLaboratoire d’Hématologie, CHU La Rabta La RabtaTunisie

Salem AbbesLaboratoire d’Hématologie Moléculaire et Cellulaire, Institut Pasteur TunisTunisie

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A New δ Chain Variant, Hb A₂-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], Observed in a Tunisian Family in Association with a Compound Heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β⁰-Thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A]

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A New δ Chain Variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], Observed in a Tunisian Family in Association with a Compound Heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β0-Thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A]

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A New δ Chain Variant, Hb A₂-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], Observed in a Tunisian Family in Association with a Compound Heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β⁰-Thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A]