Mannose binding lectin (MBL2) gene variants in siekle cell disease /
Yasmine Mohamed Amrousy
Mannose binding lectin (MBL2) gene variants in siekle cell disease / التعدد الجيني لجين المانوز الرابط اللكتيني في مرض أنيميا الخلايا المنجلية Yasmine Mohamed Amrousy ; Supervised Menat Allah Kamal Eldeen , Mervat Mamdouh Khorshied , Zainab Ali Hassan Elsadani - Cairo : Yasmine Mohamed Amrousy , 2011 - 113 P. : charts ; 25cm
Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Clinical and Chemical Pathology
Sickle cell disease (SCD) is an inherited disorder of sickle hemoglobin affecting millions of people wordwide. The current study aimed at detecting the prevalence of MBL2 exon-1 (codon 52, 54 and 57) and promoter region (-221, X/Y) genetic polymorphisms in Egyptian children with SCD to clear out its possible role as a genetic risk factor for susceptibility to venous occlusion (VOC) and/or infections
MBL2 Polymorphism Sickle cell disease
Mannose binding lectin (MBL2) gene variants in siekle cell disease / التعدد الجيني لجين المانوز الرابط اللكتيني في مرض أنيميا الخلايا المنجلية Yasmine Mohamed Amrousy ; Supervised Menat Allah Kamal Eldeen , Mervat Mamdouh Khorshied , Zainab Ali Hassan Elsadani - Cairo : Yasmine Mohamed Amrousy , 2011 - 113 P. : charts ; 25cm
Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Clinical and Chemical Pathology
Sickle cell disease (SCD) is an inherited disorder of sickle hemoglobin affecting millions of people wordwide. The current study aimed at detecting the prevalence of MBL2 exon-1 (codon 52, 54 and 57) and promoter region (-221, X/Y) genetic polymorphisms in Egyptian children with SCD to clear out its possible role as a genetic risk factor for susceptibility to venous occlusion (VOC) and/or infections
MBL2 Polymorphism Sickle cell disease