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Autor:
Okonkwo CO
Publikováno v:
Haematology International Journal. 5:1-7
Background: Sickle cell disease (SCD) is an inherited blood disorder resulting from a point mutation of thymine (T) for adenine (A) at codon 6 of the gene for beta-globin chain of haemoglobin, leading to substitution of Valine for Glutamate at positi
Autor:
Okonkwo CO; Department of Biochemistry, University of Calabar, Cross Rivers State, Nigeria., Ohaeri OC; Department of Biochemistry, Michael Okpara University of Agriculture Umudike, Abia State, Nigeria., Atangwho IJ; Department of Biochemistry, University of Calabar, Cross Rivers State, Nigeria.
Publikováno v:
Heliyon [Heliyon] 2019 May 24; Vol. 5 (5), pp. e01746. Date of Electronic Publication: 2019 May 24 (Print Publication: 2019).