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- W3118420565 abstract "Objective The explore the genetic basis for a patient with microcytic hypochromic anemia and iron deficiency anemia. Methods Common deletions and variants of the globin genes were detected by Gap-PCR and next generation sequencing (NGS). Suspected mutations were verified by Sanger sequencing. Results Gap-PCR and NGS showed that the proband has carried a αα/-α 3.7 deletion and a heterozygous c.2T>A (p.Met1Lys) mutation in the initiation codon of the HBA2 gene. The patient and her father both carried α HBA2 c.2T>A(p.Met1Lys) α/-α 3.7, while her mother and other family members were -α3.7/-α3.7 and αα/-α 3.7, respectively. Conclusion Patients with α HBA2 c.2T>A(p.Met1Lys) α/-α 3.7 genotype have typical features of thalassemia and abnormal hematologic indices compared with those with αα/-α3.7 genotype, suggesting that the HBA2 c.2T>A (p.Met1Lys) is a pathogenic variant. Above finding has enriched the spectrum of α-thalassemia mutations and enabled genetic counseling and prenatal diagnosis for the family." @default.
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- W3118420565 date "2021-01-10" @default.
- W3118420565 modified "2023-09-23" @default.
- W3118420565 title "[A case with α-thalassemia caused by novel start codon variant in conjunct with right deletion variant of α2-globin gene]." @default.
- W3118420565 doi "https://doi.org/10.3760/cma.j.cn511374-20191114-00581" @default.
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