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Haemoglobin Lepore trait: haematological and structural studies on the Italian population.

作者信息

Marinucci M, Mavilio F, Massa A, Gabbianelli M, Fontanarosa P P, Samoggia P, Tentori L

出版信息

Br J Haematol. 1979 Aug;42(4):557-65. doi: 10.1111/j.1365-2141.1979.tb01168.x.

Abstract

Haematological data on 59 heterozygotes for haemoglobin (Hb) Lepore and 10 double heterozygotes for Hb Lepore and beta thalassaemia from 36 Italian families are reported. The red cell indices are defined and compared with those of groups of non-thalassaemic and beta thalassaemic subjects of comparable number, age and sex distribution. The relative level of each haemoglobin fraction and the absolute production of single polypeptide chains are calculated in order to compare the expression of the non-alpha chain genes in Hb Lepore trait and beta thalassaemia. Structural studies demonstrate that the haemoglobin Lepore is of the Boston type (delta 87 beta 116) in all subjects, confirming that this type of fusion variant is probably the only one which occurs in Mediterranean populations. The distribution and incidence of the Lepore haemoglobinopathy are discussed.

摘要

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引用本文的文献

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Homozygous Lepore Syndrome: A case report.纯合子 Lepore 综合征:一例报告。
Ann Med Surg (Lond). 2022 Jul 14;80:104168. doi: 10.1016/j.amsu.2022.104168. eCollection 2022 Aug.

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