The Genetic Dissection of Fetal Haemoglobin Persistence in Sickle Cell Disease in Nigeria
Oyesola O. Ojewunmi,Titilope A. Adeyemo,Ajoke Oyetunji,Bassey Inyang, Afolashade Akinrindoye,Baraka S. Mkumbe,Kate Gardner,Helen Rooks,John Brewin,Hamel Patel,Sang Hyuck Lee,Raymond Chung,Sara Rashkin,Guolian Kang,Reuben Chianumba,Raphael Sangeda,Liberata Mwita,Hezekiah Isa,Uche-Nnebe Agumadu,Rosemary Ekong,Jamilu A. Faruk,Bello Y. Jamoh,Niyi M. Adebiyi,Ismail A. Umar,Abdulaziz Hassan,Christopher Grace,Anuj Goel,Baba P. D. Inusa,Mario Falchi,Siana Nkya,Julie Makani,Hafsat R. Ahmad,Obiageli Nnodu,John Strouboulis,Stephan Menzel Human Molecular Genetics（2024）
Key words
fetal haemoglobin,sickle cell disease,genome-wide association study,heritability,haplotype analysis
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