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Autor:
R Manasa Reddy1 , Srilatha K
Publikováno v:
Perspectives In Medical Research, Vol 5, Iss 3, Pp 52-56 (2017)
Background: Sickle cell haemoglobin (HbS) results from an autosomal recessively inherited mutation in which the amino-acid glutamine is replaced by valine at position 6 in the beta globin chain of haemoglobin (Hb). Sickle cells have a reduced def
Externí odkaz:
https://doaj.org/article/c4745299d6ab46628c7a133a7ba5af3c
