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Clinical and molecular genetic features of Hb H and AE Bart’s diseases in central Thai children
BACKGROUND: α-Thalassemia, one of the major thalassemia types in Thailand, is caused by either deletion or non-deletional mutation of one or both α-globin genes. Inactivation of three α-globin genes causes hemoglobin H (Hb H) disease, and the combination of Hb H disease with heterozygous hemoglobin...
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| 出版年: | Appl Clin Genet |
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| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Dove Medical Press
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5892615/ https://ncbi.nlm.nih.gov/pubmed/29662324 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TACG.S161152 |
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