Thalassemia in Southeast Asia: Determination of Different Degrees of Severity of Anemia in Thalassemia
ชื่อเรื่อง
Thalassemia in Southeast Asia: Determination of Different Degrees of Severity of Anemia in Thalassemia
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ผู้สร้าง/เจ้าของผลงาน
Wasi, Prawase
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Pootrakul, Pensri
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Fucharoen, Suthat
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Winichagoon, Pranee
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Wilairat, Prapon
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Promboon, Amornrat
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หัวเรื่อง
History and Philosophy of Science
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General Biochemistry, Genetics and Molecular Biology
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General Neuroscience
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คำอธิบายรายละเอียดของเอกสาร
This study was supported by US Public Health research grant AM 09805 from the National Institute of Arthritis, Diabetes, Digestive and Kidney Diseases.
บทคัดย่อ
In Southeast Asia, a-thalassemias, P-thalassemia, hemoglobin (Hb) E and Hb Constant Spring are prevalent.'-3 The a-thalassemias consist of two common alleles, that is, a-thalassemia 1 occurring from deletion of two adjacent structural a-globin genes and a-thalassemia 2 occurring from DNA defects equivalent to deletion of one a-globin gene. The combined frequencies of a-thalassemia 1 and a-thalassemia 2 are 20-30 percent. p-thalassemia predominates over P+-thalassemia by a wide margin, and its frequencies vary from 3 to 9 percent. Hb E is frequent up to 50-60 percent in certain areas. Hb Constant Spring frequencies vary from a few percentage points to 8 percent. These genes form complex thalassemia syndromes.
ผู้ร่วมงาน
Mahidol University Faculty of Medicine, Siriraj Hospital
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ปีที่ผลิตเอกสาร
วันที่บันทึกข้อมูล
2023-05-02
ประเภท
Article
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รูปแบบ
ขนาดหรือจำนวนของเอกสาร
8 pages
ต้นฉบับ/แหล่งที่มาของเอกสาร
Annals of the New York Academy of Sciences ; volume 445, issue 1 Fifth Cooley, page 119-126
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รหัส หรือตัวบ่งชี้เอกสาร
ขอบเขต
เจ้าของลิขสิทธิ์
John Wiley & Sons, Inc.
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