Literature DB >> 4061450

Five adults with mild sickle cell anemia share a beta S chromosome with the same haplotype.

I Bakioglu, Y Hattori, A Kutlar, C Mathew, T H Huisman.   

Abstract

Five adult SS patients from Qatar, Turkey, and South Africa with mild disease, had greatly elevated Hb F and specific patterns of polymorphic sites on their beta S chromosomes. One subject had an alpha-thalassemia (-alpha/-alpha). The haplotypes were the common type #19, associated with severe disease, and type #31, not seen thus far in an SS patient (numbering system of Antonarakis et al). The data suggest that modifications in the DNA of the beta S #31 chromosome promotes the synthesis of gamma chains.

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Year:  1985        PMID: 4061450     DOI: 10.1002/ajh.2830200313

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  3 in total

1.  Geographical survey of beta S-globin gene haplotypes: evidence for an independent Asian origin of the sickle-cell mutation.

Authors:  A E Kulozik; J S Wainscoat; G R Serjeant; B C Kar; B Al-Awamy; G J Essan; A G Falusi; S K Haque; A M Hilali; S Kate
Journal:  Am J Hum Genet       Date:  1986-08       Impact factor: 11.025

2.  The levels of zeta, gamma, and delta chains in patients with Hb H disease.

Authors:  F Kutlar; J M Gonzalez-Redondo; A Kutlar; A Gurgey; C Altay; G D Efremov; K Kleman; T H Huisman
Journal:  Hum Genet       Date:  1989-05       Impact factor: 4.132

Review 3.  Sickle cell disease in Middle East Arab countries.

Authors:  Mohsen A F El-Hazmi; Ali M Al-Hazmi; Arjumand S Warsy
Journal:  Indian J Med Res       Date:  2011-11       Impact factor: 2.375

  3 in total

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