Fig. 3From: A Chinese patient with developmental and epileptic encephalopathies (DEE) carrying a TRPM3 gene mutation: a paediatric case reportSequencing of the TRPM3 gene: c.3605G > C (p.S1202T). The child has a heterozygous Mutation, and his parents are normal. (a patient; b the father; c the mother)Back to article page