Fig. 3From: An infantile case of hereditary folate malabsorption with sudden development of pulmonary hemorrhage: a case reportElectropherograms of c.1166-285T>G mutation for the patient and his parents. Sequence genomic deoxyribonucleic acid targeting c.1166-285T>G shows homozygosity of the mutation in the patient. His parents were heterozygous for the mutation. A adenine, G guanine, T thymine, C cytosineBack to article page