Fig. 1From: Identification of mutations that causes glucose-6-phosphate transporter defect in tunisian patients with glycogenosis type 1bFamily pedigree and electropherograms showing the reported mutation p.R300H and p.W393X associated with Glycogen storage disease type 1b(a) The right and left panel indicate the sequence electropherogram of the SLC37A4 mutations identified in exon 6 and 9 in the patients with GSD1b, respectively. (b) The right, the middle and the left panel concern the family pedigree of the patient MT, MB, and SI, respectivelyBack to article page