Fig. 2From: CAD gene and early infantile epileptic encephalopathy-50; three Iranian deceased patients and a novel mutation: case reportChromatogram in the father (A) and mother (B) of the patients are showing the c.2995G > A (p.V999M) mutation in CAD gene in heterozygous states. The chromatogram in the affected child (C) shows the mutation in a homozygous stateBack to article page