The First Report of a 290-bp Deletion in β-Globin Gene in the South of Iran.

Mohammad Hamid,Ladan Dawoody Nejad,Gholamreza Shariati,Hamid Galehdari,Alihossein Saberi,Marziye Mohammadi-Anaei

Iranian biomedical journal（2017）

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摘要

This mutation causes β0-thalassemia and can be highly useful for prenatal diagnosis in compound heterozygous condition with different β-globin gene mutations.

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关键词

β-thalassemia,β-globin gene mutation,Iran,Multiplex ligation-dependent probe ampliﬁcation

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