Figure 2
From: Association between coenzyme Q10 and glucose transporter (GLUT1) deficiency
Genetic analysis. A- Electropherogram containing genomic SLC2A1 DNA mutation in a case with GLUT1 deficiency. B- 3% agarose gel showing a 219 base pairs PCR amplification of SLC2A1 cDNA region enconmpassing the spling mutation. C (control) and P (patient). C- Patient's electropherograms showing a synonymous polymorphism (rs1385129, see dbSNP database) in heterozygous state in gDNA and in hemizygous state in cDNA.