β globin mutations in Turkish, Northern Iraqi and Albanian patients with β thalassemia major
The mutation detection of β thalassemia is absolutely necessary for molecular diagnosis, as well as any genetic epidemiological study. The β globin gene has 3 exons and 2 introns, involved in β-thalassemic pathogenesis. The study aim of the study is to characterize the spectrum of β globin gene muta...
保存先:
| 主要な著者: | , , , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
MDPI AG
2018-06-01
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| シリーズ: | Thalassemia Reports |
| 主題: | |
| オンライン･アクセス: | https://www.pagepressjournals.org/index.php/thal/article/view/7286 |
| タグ: |
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