Association of Xmn1 −158 γG variant with severity and HbF levels in β-thalassemia major and sickle cell anaemia-Reference-Cited by-同舟云学术

Association of Xmn1 −158 γG variant with severity and HbF levels in β-thalassemia major and sickle cell anaemia

Published:2014-02-02 Issue:5 Volume:41 Page:3331-3337
ISSN:0301-4851
Container-title:Molecular Biology Reports
language:en
Short-container-title:Mol Biol Rep

Author:

Dadheech Sneha,Jain Suman,Madhulatha D.,Sharma Vandana,Joseph James,Jyothy A.,Munshi Anjana

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s11033-014-3195-5.pdf

Reference32 articles.

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2. Nagel RL, Platt OS (2001) General pathophysiology of sickle cell anemia. In: Steinberg MH, Forget BG, Higgs DR, Nagel RL (eds) Disorders of hemoglobin: genetics, pathophysiology, and clinical management. Cambridge University Press, Cambridge, pp 494–526

3. Verma IC (2000) Burden of genetic disorders in India. Indian J Pediatr 67:893–898

4. International Committee for Standardization in Haemotology (1978) Recommendations for selected methods for quantitative estimation of HbA2 and HbA2 reference preparation. Br J Haematol 38:573–578

5. Gilman JG, Huisman THJ (1985) DNA sequence variation associated with elevated fetal Gg globin production. Blood 66:783–787

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