doi: 10.1126/science.156.3773.397.
"Hemoglobin alpha2beta2-121ys" chemical identification in an egyptian family
- PMID:5609824
- DOI: 10.1126/science.156.3773.397
Item in Clipboard
"Hemoglobin alpha2beta2-121ys" chemical identification in an egyptian family
K A Kamel et al. Science..
Display options
Format
Display options
Format
Abstract
Stuidy of the amino acid composition and amino-terminal residue in the abnormal peptide of an electrophoretically slow hemoglobin revealed that the globin's structure was alpha(2)beta(2)(121 Lys) (Obeta). This hemoglobin had been provisionally classified as Hb E or as a new heemoglobin. The clinical significance of this abnormality is not yet defined.
Similar articles
- A new hemoglobin variant resembling hemoglobin E. Hemoglobin E Saskatoon: beta-22 Glu replaced by Lys.Vella F, Lorkin PA, Carrell RW, Lehmann H.Vella F, et al.Can J Biochem. 1967 Sep;45(9):1385-91. doi: 10.1139/o67-163.Can J Biochem. 1967.PMID:6048388No abstract available.
- Haemoglobin Leiden: deletion of beta-6 or 7 glutamic acid.De Jong WW, Went LN, Bernini LF.De Jong WW, et al.Nature. 1968 Nov 23;220(5169):788-90. doi: 10.1038/220788a0.Nature. 1968.PMID:5698750No abstract available.
- Hemoglobin Hijiyama: a new fast-moving hemoglobin in a Japanese family.Miyaji T, Oba Y, Yamamoto K, Shibata S, Iuchi I, Hamilton HB.Miyaji T, et al.Science. 1968 Jan 12;159(3811):204-6. doi: 10.1126/science.159.3811.204.Science. 1968.PMID:5634912
- Two variants of hemoglobin D in the algerian population: hemoglobin D Ouled Rabah 19 (BI) Asn leads to Lys and hemoglobin D Iran 22 (Br) Glu leads to Gln.Elion J, Belkhodja O, Wajcman H, Labie D.Elion J, et al.Biochim Biophys Acta. 1973 Jun 15;310(2):360-4. doi: 10.1016/0005-2795(73)90117-7.Biochim Biophys Acta. 1973.PMID:4719147No abstract available.
- Characterization of the alpha chain core of human haemoglobin variants.Carrell RW, Irvine D.Carrell RW, et al.Biochim Biophys Acta. 1968 Jan 22;154(1):78-83. doi: 10.1016/0005-2795(68)90260-2.Biochim Biophys Acta. 1968.PMID:5639028No abstract available.
Cited by
- The interaction of hemoglobin O Arab with Hb S and beta+ thalassemia among Israeli Arabs.Rachmilewitz EA, Tamari H, Liff F, Ueda Y, Nagel RL.Rachmilewitz EA, et al.Hum Genet. 1985;70(2):119-25. doi: 10.1007/BF00273069.Hum Genet. 1985.PMID:3859465
- Haemoglobin O Arab (B121 Glu-Lys) in Turkish Cypriot population.Cin S, Akar N, Arcasoy A, Cavdar AO, Dedeoğlu S.Cin S, et al.J Med Genet. 1984 Apr;21(2):158. doi: 10.1136/jmg.21.2.158.J Med Genet. 1984.PMID:6716421Free PMC article.No abstract available.
MeSH terms
Substances
Related information
LinkOut - more resources
Full Text Sources