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Article

Complex Interaction of Hb Q-Thailand with α and β Thalassemia in a Hakka Family

2020-03-12

Abstract excerpt

<title>Abstract</title> <p>Background HbQ-Thailand is an α-globin chain variant that results from a point mutation at codon 74 of the α1-globin gene on chromosome 16p. It commonly appears with a leftward single α-globin gene deletion (-α 4.2 ). There have been few reports regarding the interaction between HbQ-Thailand and other globin gene disorders. Here we found and diagnosed it in the Hakka population of the F...

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Literature Corpus work
08e3093a-d45e-5112-b3a8-52ffec18346b
DOI
10.21203/rs.3.rs-17041/v1
Open publication

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Complex Interaction of Hb Q-Thailand with α and β Thalassemia in a Hakka FamilyDOI 10.21203/rs.3.rs-17041/v1
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