Hematological and Molecular Characterization of Hb J-Buda [α61(E10)Lys → Asn, AAG > AAT]
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
http://link.springer.com/content/pdf/10.1007/s12288-016-0641-7.pdf
Reference8 articles.
1. Achoubi N, Asghar M, Saraswathy KN, Murry B (2012) Prevalence of beta-thalassemia and hemoglobin E in two migrant populations of Manipur, North East India. Genet Test Mol Biomark 16(10):1195–1200
2. Giardine B, Borg J, Viennas E, Pavlidis C, Moradkhani K, Joly P et al (2014) Updates of the HbVar database of human hemoglobin variants and thalassemia mutations. Nucleic Acids Res 42(Database issue):D1063–D1069. doi: 10.1093/nar/gkt911
3. Piel FB, Weatherall DJ (2014) The alpha-thalassemias. N Engl J Med 371(20):1908–1916
4. Itchayanan D, Svasti J, Srisomsap C, Winichagoon P, Fucharoen S (1999) Identification of Hb J-Buda [alpha61(E10)Lys → Asn] in a Thai female. Hemoglobin 23(2):183–186
5. Hollan SR, Szelenyi JG, Brimhall G, Duerst M, Jones RT, Koler RD et al (1972) Multiple alpha chain loci for human haemoglobins: Hb J-Buda and Hb G-Pest. Nature 235(5332):47–50
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1. α-Thalassemia Intermedia Results from Interactions of Unstable Hb Prato [α31(B12)Arg→Ser (HBA1 or HBA2 c.96G>T or C)] with the α-Thalassemia-1 [– –SEA (Southeast Asian)] Deletion in Thailand;Hemoglobin;2020-07-03
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