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Fig. 3 | BMC Medical Genetics

Fig. 3

From: Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania

Fig. 3

Biological sub-network of the candidate mutant gene and identified modifier genes in 14 SCD patients from Tanzania. a sub-networks of the mutant gene and identified candidate genetic modifiers include CHD4 and MBD3. b description of the top most significant pathways, GO biological process, and Human Phenotypes associated with the identified variants

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