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Hemoglobin
international journal for hemoglobin research
Volume 26, 2002 - Issue 1
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Hb SIAM [α15(A13)Gly → Arg (α1) (GGT → CGT)] IS A TYPICAL α CHAIN HEMOGLOBINOPATHY WITHOUT AN α-THALASSEMIC EFFECT

Chairat Turbpaiboon Department of Biochemistry, Faculty of Science, Mahidol University, Rama 6 Road, Bangkok, 10400, Thailand
,
Saovaros Svasti Thalassemia Research Center, Institute of Science and Technology for Research and Development, Mahidol University, Salaya, Nakorn Pathom, 73170, Thailand
,
Phannee Sawangareetakul Laboratory of Biochemistry, Chulabhorn Research Institute, Bangkok, 10210, Thailand
,
Pranee Winichagoon Thalassemia Research Center, Institute of Science and Technology for Research and Development, Mahidol University, Salaya, Nakorn Pathom, 73170, Thailand
,
Chantragan Srisomsap Laboratory of Biochemistry, Chulabhorn Research Institute, Bangkok, 10210, Thailand
,
Noppadol Siritanaratkul Department of Medicine, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, 10700, Thailand
,
Suthat Fucharoen Thalassemia Research Center, Institute of Science and Technology for Research and Development, Mahidol University, Salaya, Nakorn Pathom, 73170, Thailand
,
Prapon Wilairat Department of Biochemistry, Faculty of Science, Mahidol University, Rama 6 Road, Bangkok, 10400, Thailand
&
Jisnuson Svasti Department of Biochemistry, Faculty of Science, Mahidol University, Rama 6 Road, Bangkok, 10400, Thailand; Laboratory of Biochemistry, Chulabhorn Research Institute, Bangkok, 10210, Thailand
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Pages 77-81 | Received 19 Jun 2001, Accepted 21 Aug 2001, Published online: 07 Jul 2009

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Agathe Horri-Naceur & David J. Timson. (2020) In Silico Analysis of the Effects of Point Mutations on α-Globin: Implications for α-Thalassemia. Hemoglobin 44:2, pages 89-103.
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Articles from other publishers (4)

Pankaj Kumar, Amit Bugalia, Pallavi Thaker, Manju Gorivale, Nighat Hussain, Anita Nadkarni & Nabhajit Mallik. (2022) Co-inheritance of Hb Ottawa and HbS: a rare interaction leading to an interesting diagnostic challenge. Journal of Hematopathology 15:4, pages 271-273.
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Ru‐Qing Zhao, Fan Jiang, Jian Li, Jian‐Ying Zhou, Xue‐Wei Tang, Fa‐Tao Li, Li‐Qiong Chen & Dong‐Zhi Li. (2021) A novel SPTB frameshift deletion causing hereditary spherocytosis identified by next‐generation sequencing in a Chinese family. International Journal of Laboratory Hematology 43:6.
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Beverley M. Pullon & Jordyn A. Moore. (2020) Hemoglobin Ottawa (HBA2:c.46G>C) and β+ Thalassemia (HBB:c.-138C>T) Detected in an Indian Male by Capillary Zone Electrophoresis. Thalassemia Reports 10:1, pages 8733.
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Mariana F. Nery, José Ignacio Arroyo & Juan C. Opazo. (2013) Genomic Organization and Differential Signature of Positive Selection in the Alpha and Beta Globin Gene Clusters in Two Cetacean Species. Genome Biology and Evolution 5:12, pages 2359-2367.
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