Hemoglobin Siam α2 15argβ2: A new α-chain variant
ชื่อเรื่อง
Hemoglobin Siam α2 15argβ2: A new α-chain variant
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ผู้สร้าง/เจ้าของผลงาน
Pootrakul, Sa-nga
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Srichiyanont, Sithichai
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Wasi, Prawase
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Suanpan, Suparb
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หัวเรื่อง
Genetics (clinical)
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Genetics
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บทคัดย่อ
A 28-year-old, healthy male of chinese ancestry with normal hematologic findings was found to have an abnormal hemoglobin moving more slowly than hemoglobin F in starch gel electrophoresis. The relative amounts of the abnormal component, hemoglobin A2 and slow hemoglobin A2, as determined by cellulose acetate electrophoresis, were 15.2, 1.64, and 0.56% respectively. The hemoglobin chain dissociation by p-chloromercuribenzoate treatment confirmed that it was an α-chain variant. The abnormal globin chain was fractionated by carboxymethyl cellulose chromatography. Peptide mapping revealed that the amino acid alteration occurs in αTp III (tryptic peptide No. 3, residues 12 to 16 of the α-chain). Special stains and amino acid analyses of the abnormal peptide indicated that glycine at residue 15 was replaced by arginine, and the hemoglobin is thus α2 15argβ2. Since the mutation has not been previously described, it is proposed that it be called “Hemoglobin Siam”.
ผู้ร่วมงาน
Division of Hematology, Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand
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Nutrition Division, Department of Public Health Promotion, Ministry of Public Health, Bangkok, Thailand
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ปีที่ผลิตเอกสาร
วันที่บันทึกข้อมูล
2023-05-01
ประเภท
Article
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รูปแบบ
ขนาดหรือจำนวนของเอกสาร
6 pages
ต้นฉบับ/แหล่งที่มาของเอกสาร
Humangenetik, Vol, 23, Page 199–204
ภาษา
รหัส หรือตัวบ่งชี้เอกสาร
ขอบเขต
เจ้าของลิขสิทธิ์
Springer Nature Switzerland AG. Part of Springer Nature.
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