Fig. 4From: A newborn with seizures born to a mother diagnosed with primary carnitine deficiencyMutation sites for c.1400C > G of the SLC22A5. a is for reference. The newborn had a heterozygote mutation for c.1400C > G of the SLC22A5 gene (b). Her mother had a homozygous mutation for c.1400C > G (c). Her father had normal SLC22A5 gene. The red arrows show mutation site (d)Back to article page