Hb Hinwil [β38(C4)Thr→Asn, ACC>AAC] Associated with β⁰-Thalassemia in a Sicilian Child

Liana Cuccia Unità Operativa Complessa Ematologia-Emoglobinopatie, P.O. “G. Di Cristina”, Palermo, ItaliaCorrespondence[email protected]

Laura Saieva Unità Operativa Complessa Ematologia-Emoglobinopatie, P.O. “G. Di Cristina”, Palermo, Italia

Zelia Borsellino Unità Operativa Complessa Ematologia-Emoglobinopatie, P.O. “G. Di Cristina”, Palermo, Italia

Maria R. Marocco Unità Operativa Complessa Ematologia-Emoglobinopatie, P.O. “G. Di Cristina”, Palermo, Italia

Giovan B. Ruffo Unità Operativa Complessa Ematologia-Emoglobinopatie, P.O. “G. Di Cristina”, Palermo, Italia

Jean Riou Department of Genetic Biochemistry, Hôpital Henri Mondor, Créteil France

Marcello Capra Unità Operativa Complessa Ematologia-Emoglobinopatie, P.O. “G. Di Cristina”, Palermo, Italia

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Hb Hinwil [β38(C4)Thr→Asn, ACC>AAC] Associated with β⁰-Thalassemia in a Sicilian Child

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Hb Hinwil [β38(C4)Thr→Asn, ACC>AAC] Associated with β0-Thalassemia in a Sicilian Child

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Hb Hinwil [β38(C4)Thr→Asn, ACC>AAC] Associated with β⁰-Thalassemia in a Sicilian Child